F 0552
Ensure that residents are fully informed and understand their health status, care and treatments.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and medical record review, the facility failed to ensure one of 13 final sampled residents (Resident
330) was informed in advance of the proposed treatment regarding the use of psychotropic medications
(medications affecting brain activity).
Residents Affected - Few
* The facility failed to ensure the informed consent was obtained from Resident 330's responsible party
before administering sertraline (antidepressant medication) to Resident 330. This failure had the potential to
compromise the right of the resident or her responsible party (person designated to make decisions on
behalf of the resident) to be fully informed regarding the medication and its potential side effects.
Findings:
Medical record review for Resident 330 was initiated on 1/23/24. Resident 330 was readmitted to the facility
on [DATE].
Review of Resident 330's History and Physical examination dated 1/15/24, showed Resident 330 had no
capacity to understand and make decisions.
Review of the Order Summary Report showed a physician's order dated 1/16/24, to administer sertraline 50
mg one tablet a day for depression manifested by verbalization of sadness.
Review of the Consent Form for Psychoactive Med Therapy dated 1/12/24, did not show the sertraline
medication ordered.
Review of the Informed Consent Form - Skilled Nursing (CA Only) dated 1/16/24, did not show the
sertraline medication ordered.
Further review of Resident 330's medical record did not show documented evidence of informed consent
for the sertraline medication was obtained from Resident 330's responsible party.
On 1/26/24 at 1008 hours, an interview and concurrent medical record review for Resident 330 was
conducted with the DON. The DON verified the above findings. The DON verified the informed consent
forms did not show the sertraline medication ordered for Resident 330. The DON acknowledged the
informed consent forms were incomplete.
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 74
Event ID:
555768
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0558
Reasonably accommodate the needs and preferences of each resident.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, medical record review, and facility P&P review, the facility failed to provide the
reasonable accommodation to meet the needs of one of 13 final sampled residents (Resident 8).
Residents Affected - Few
* The facility failed to ensure the call light for Residents 8 was within the resident's reach. This had the
potential for the resident to not be able to call for assisstance when needed.
Finding:
Review of the facility's P&P titled Answering Call Light revised September 2022 showed the facility should
ensure the call light is accessible to the resident when in bed, from the toilet, from the shower, from the
shower or bathing facility & from the floor.
During the initial tour of the facility on 1/23/24 at 1047 hours, Resident 8 was observed lying in her bed,
awake, with the call light hanging on a metal rod on the right side of the head of bed.
Medical record review for Resident 8 was initiated on 1/23/24. Resident 8 was admitted to the facility on
[DATE].
Review of Resident 8's History and Physical examination dated 10/13/23, showed Resident 8 had no
capacity to understand and make her own decisions.
On 1/23/24 at 1055 hours, an observation and concurrent interview was conducted with CNA 1. CNA 1
verified Resident 8's call light was not within reach. CNA 1 stated Resident 8's call light should have been
within the resident's reach. CNA 1 also stated the call light should always be within the reach of all the
residents while they were in bed whether they were alert and oriented or confused.
On 1/25/24 at 0855 hours, an interview was conducted with the DON. The DON stated the expectation was
for the call light to be placed within reach of the residents even if the residents were confused. The DON
stated their call light system was very sensitive also for the movements. If the resident was restless,
constantly moving or trying to get out of bed, the call light helped to alert the staff to check on the resident.
The DON was informed and acknowledged the above findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 2 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0578
Level of Harm - Minimal harm
or potential for actual harm
Honor the resident's right to request, refuse, and/or discontinue treatment, to participate in or refuse to
participate in experimental research, and to formulate an advance directive.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Medical
record review for Resident 25 was initiated on 1/24/24. Resident 25 was admitted to the facility on [DATE].
Residents Affected - Few
Review of Resident 25's History and Physical examination dated 12/29/23, showed Resident 25 did not
have the capacity to understand, and make decisions.
Review of Resident 25's Generations Care Conference dated 12/28/23, showed Resident 25 was admitted
to the facility with an advanced directives.
Review of Resident 25's POLST dated 12/28/23, under Section D-Information and Signatures, showed
Resident 25 did not have an advance directive.
Review of Resident 25's medical record failed to show documented evidence a copy of Resident 25's
advance directive was obtained or a follow-up was made to obtain a copy of Resident 25's advance
directive as per the facility's P&P.
On 1/24/24 at 1445 hours, an interview and concurrent medical record review was conducted with the SSD.
The SSD verified the medical record did not contain a copy of Resident 25's advance directive.
On 1/24/24 at 1615 hours, an interview and concurrent medical record review was conducted with the
DON. The DON was informed and verified the above findings.
Based on interview, medical record review, and facility P&P review, the facility failed to ensure the residents'
advance directives were part of their medical records for three of 13 final sampled residents (Residents 19,
25, and 429). This failure had the potential for the residents' wishes for provisions of health care not being
followed.
Findings:
Review of the facility's P&P titled ADM- Advanced Directives dated 9/1/22, showed upon admission, the
facility will ask the resident or the resident's representative if they have an Advance Directive, and copies
are obtained and maintained in the residents' medical record.
1. Medical record review for Resident 429 was initiated on 1/23/24. Resident 429 was admitted to the facility
on [DATE].
Further review of Resident 429's medical record failed to show a POLST and if the resident had an
advance directive.
Review of Resident 429's Generations Care Conference -V3 dated 1/17/23, the section for advance
directive was incomplete.
On 1/24/24, at 1009 hours, an interview and concurrent medical record review was conducted with LVN 4.
LVN 4 stated they were the admitting nurse for Resident 429, and the LVN filled out a POLST for the
resident. LVN 4 stated Resident 429's family member provided him a copy of the resident's advance
directive on admission and they should both (POLST and advance directive) be in the binder at the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 3 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0578
Level of Harm - Minimal harm
or potential for actual harm
station. Review of the binder labeled Facesheets, POLSTS, Inventory Records with LVN 4, LVN 4 verified
Resident 429's POLST and advanced directive were not located in the binder.
On 1/24/24, an interview was conducted with the SSD. The SSD stated Resident 429 informed her that he
believed he had an advance directive and to ask Family Member 1.
Residents Affected - Few
On 1/24/24 at 1132 hours, an interview was conducted with Family Member 1. Family Member 1 stated they
provided a copy of Resident 429's advance directive to the nurse on admission, and the facility should have
a copy of it.
2. Medical record review for Resident 19 was initiated on 1/23/24. Resident 19 was initially admitted to the
facility on [DATE]. Review of the Resident - POLST dated 12/11/23, showed the resident did not have an
advance directive.
Review of Resident 19's admission MDS dated [DATE], showed the resident was cognitively intact.
On 1/23/24 at 1211 hours, an interview was conducted with Resident 19. Resident 19 stated they had an
advance directive and stated the facility was provided a copy of it.
Review of Resident 19's medical record failed to show a copy of Resident 19's advance directive.
Review of Resident 19's Generations Care Conference -V3 dated 12/10/23, showed the resident did not
have an advance directive.
Review of Resident 19's Physician Orders for Life-sustaining Treatment (POLST) dated 12/11/23, showed
the resident did not have an advance directive.
On 1/24/24 at 1012 hours, an interview and concurrent medical record review was conducted with LVN 4.
LVN 4 reviewed Resident 19's POLST and stated it showed the resident did not have an advance directive.
LVN 4 reviewed Resident 19's medical record and verified there was no advance directive.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 4 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0580
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Immediately tell the resident, the resident's doctor, and a family member of situations (injury/decline/room,
etc.) that affect the resident.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview, medical record review, and facility P&P review, the facility failed to ensure the timely notification of
changes for one of 13 final sampled residents (Resident 16).
* The facility failed to notify the physician, RD, and resident responsible party for the resident's weight
changes. This failure had the potential for a delay of the interventions to prevent further weight loss/gain.
Findings:
Review of the facility's P&P Weight Assessment and Intervention dated 12/1/22, showed the following:
- A weight change of 5% or more since prior weight assessment will be rechecked the next day, and if
verified, nursing will immediately notify the dietitian.
- Unless notified of a significant weight change (5% weight loss in a one month period; greater than 5% is
severe weight loss.)
Review of the facility's P&P Change in a Resident's Condition or Status revised 2/2021 showed the facility
promptly notifies the resident's physician and responsible party of changes in the resident's medical status,
including for significant changes in the resident's physical condition. The nurse will record the notification in
the resident's medical record.
Medical record review for Resident 16 was initiated on 1/23/24. Resident 16 was admitted to the facility on
[DATE]. Review of Resident 16's admission Record showed Resident 16's primary emergency contact was
Family Member 2.
Review of Resident 16's Weight and Vitals Summary in the resident's electronic medical record dated
1/24/24, showed the following weights:
- 148.2 lbs, on 12/4/23,
- 142.6 lbs, on 12/19/23,
- 150 lbs, on 12/26/23 (5.2% and 7.4 lbs. increase from 12/19/24's weight),
- 134.8 lbs, on 1/2/24 (10.1% and 15.2 lbs. decrease from 12/26/23's weight), and
- 139.2 lbs, on 1/9/24.
Review of Resident 16's Weight Record showed the following weights:
-148.2 lbs, on 12/4/23,
-142.6 lbs, on 12/19/23,
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 5 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0580
-134.8 lbs, on 1/2/24, and
Level of Harm - Minimal harm
or potential for actual harm
-139.2 lbs, on 1/9/24, with written notes of weight gain dated 1/10/24, and positive edema (swelling caused
by too much fluid trapped in the body's tissues)
Residents Affected - Few
The weight record did not show the resident's weight obtained on 12/26/23.
Review of Resident 16's Order Audit Report dated 1/26/24, showed on 1/4/24 at 2121 hours, a physician's
order was obtained to refer to the RD for recent weight loss, 142.6 lbs on 12/19/23, and 134.8 on 1/2/24.
The order was obtained two days after the most recent weight was obtained.
On 1/25/24 at 1414 hours, an interview and concurrent record review were conducted with CNA 1. CNA 1
stated they weighted all the residents weekly and wrote it down on the Weekly Weights log, then recorded
the weights in the resident's weight record and electronic medical record. CNA 1 stated they then gave the
weight record to the resident's nurse if there were changes, so the nurse could do a change of condition.
CNA 1 stated the nurse usually had their initials on the weight record to show they had reviewed it. When
asked why Resident 16's weight on 12/26/23, was not recorded on their weekly weight record, CNA 1
stated they must have forgotten.
Review of Resident 16's eINTERACT Change in Condition Evaluation - V 5.1 dated 1/3/24, showed an
incomplete assessment for a weight loss. The sections for reviewing the findings with the physician showed
the physician's recommendation and responsible party notification sections were blank.
Review of Resident 16's progress notes failed to show the physician was notified of Resident 16's weight
gain on 12/26/23, and was notified timely of Resident 16's weight loss on 1/2/24. The progress notes also
failed to show the RD and Resident 16's responsible party were notified of the weight changes.
On 1/25/24 at 1434 hours, an interview and concurrent medical record review were conducted with LVN 4.
LVN 4 stated for the notification of changes, to notify the physician and the resident's responsible party
immediately; and if needed, the physician would order an RD consult. LVN 4 reviewed Resident 16's Weight
and Vitals Summary and verified Resident 16's weight gain on 12/26/23, and weight loss on 1/2/24. LVN 1
was unable to find documentation to show the physician, RD, and resident's representative were notified of
the resident's weight gain. LVN 1 was unable to find documentation showing the 1/2/24 weight loss with
timely notification to the physician and that the RD and resident's responsible party were notified.
On 1/26/24 at 1112 hours, a telephone interview was conducted with Family Member 2. Family Member 2
stated they were Resident 16's primary emergency contact. Family Member 2 stated they were not notified
by the facility of any weight gain or losses.
On 1/26/24 at 1238 hours, a telephone interview was conducted with Resident 16's physician, Physician 1.
Physician 1 stated he was notified of a weight gain and reviewed the resident's weight log. When asked if it
was the weight on 1/9/24, with the note for positive edema, the physician stated yes, and that they wrote
the note about edema.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 6 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0655
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Create and put into place a plan for meeting the resident's most immediate needs within 48 hours of being
admitted
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview, medical record review, and facility P&P review, the facility failed to ensure the baseline care plans
related to the fall risk was developed for one of 13 final sampled residents (Resident 379). This failure had
the potential for the resident to not receive the necessary care and services in accordance with their care
needs.
Findings:
Review of the facility's P&P titled Baseline Care Plans for New Residents dated 6/22 showed the baseline
care plans should be completed upon admission based on the resident's individual needs.
Medical record review for Resident 379 was initiated on 1/24/24. Resident 379 was admitted to the facility
on [DATE].
Review of Resident 379's Order Summary Report for January 2024 showed a physician's order dated
1/22/24, to place the bilateral floor mats to prevent and/or minimize further injury from fall, and another
physician's order for Joerns deluxe assist handle (a assistive device attached to the resident's bedframe to
assist with mobility) times two for better positioning and transfers.
Review of the Generations Post-Acute admission Data Collection dated 1/22/24, under the section Interim
Care Plan on Falls, showed no information if Resident 379 was at risk for falls.
Review of the Morse Fall Risk assessment dated [DATE], showed Resident 379 was assessed as a low risk
for falling.
Review of the baseline plan of care formulated upon admission of Resident 379 showed the specific care
plans addressing the basic care needs of the resident. However, further review of the plan of care showed
no documented evidence a baseline care plan was developed to address the fall risk, use of side rails, and
bilateral floor mats.
On 1/24/24 at 1400 hours, an interview for Resident 379 was conducted with CNA 4. CNA 4 verified
Resident 379 had side rails installed on their bed. CNA 4 stated Resident 379 was not able to use the side
rails in bed.
On 1/25/24 at 1012 hours, an interview and concurrent medical record review for Resident 379 was
conducted with LVN 4. LVN 4 verified there was a physician's order for Resident 379's use of side rails in
bed and the floor mat on both side of the bed. LVN 4 stated Resident 379 was not able to move in bed due
to pain. LVN 4 verified Resident 379 was assessed for a low risk for fall and the least restrictive intervention
included a floor mat. LVN 4 verified there was no baseline care plan addressing the risk for fall with the use
of side rail and floor mats.
On 1/25/24 at 1019 hours, an interview and concurrent medical record review for Resident 379 was
conducted with RN 1. RN 1 verified there was a physician's order for the use of the side rail. RN 1 verified
there was no baseline care plan for fall and the use of the side rails in bed.
On 1/25/24 at 1606 hours, an interview for Resident 379 was conducted with the DON. The DON was
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 7 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0655
informed and verified the above findings.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 8 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Medical
record review for Resident 330 was initiated on 1/23/24. Resident 330 was readmitted to the facility on
[DATE].
Review of the Order Summary Report showed a physician's order dated 1/16/24, to administer sertraline 50
mg one tablet a day for depression manifested by verbalization of sadness.
Review of Resident 330's plan of care failed to show a care plan problem was developed to address
Resident 330's use of the sertraline medication.
On 2/11/22 at 0825 hours, an interview and concurrent medical record review was conducted with LVN 4.
LVN 4 stated the residents' care plans were initiated on admission and revised when there were any
changes to the resident's condition and treatment plan. LVN 4 reviewed Resident 330's care plan and
verified the above findings.
On 1/24/24 at 1542 hours, an interview and concurrent medical record review for Resident 330 was
conducted with RN 1. RN 1 verified the above findings. RN 1 stated the nurse who placed the physician's
order for the sertraline medication should have initiated the care plan for the medication.
Based on interview, medical record review, and facility P&P review, the facility failed to develop the
comprehensive care plans to reflect the individual care needs for three of 13 final sampled residents
(Resident 25, 330, and 679) when:
* The facility failed to develop a comprehensive care plan for Resident 25's use of Risperdal (a medication
used to treat a number of mental health disorders including psychosis.) and sertraline hcl (a medication
used to treat certain mood disorders such as depression.)
* The facility failed to develop a care plan problem to address Resident 330's use of sertraline hcl.
* The facility failed to develop a care plan problem to address the PVR monitoring for Resident 679.
These failures posed the risk of not providing the appropriate, consistent, and individualized care to the
residents.
Findings:
1. Review of the facility's P&P titled Care Plans, Comprehensive Person-Centered revised March 2022
showed the comprehensive, person-care plan that includes measurable objectives and timetables to meet
the resident's physical, psychosocial and functional needs is developed and implemented for each resident.
The comprehensive, person-centered care plan:
a. includes measurable objectives and timeframes;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 9 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0656
b. describes the services that are to be furnished to attain or maintain the resident's highest practicable
physical, mental, and psychosocial well-being;
Level of Harm - Minimal harm
or potential for actual harm
c. includes the resident's stated goals upon admission and desired outcomes;
Residents Affected - Few
d. builds on the resident's strengths; and
e. reflects currently recognized standards of practice for problem areas and conditions.
Medical record review for Resident 25 was initiated on 1/24/24. Resident 25 was admitted to the facility on
[DATE].
Review of Resident 25's Order Summary Report for December 2023 showed a physician's order dated
12/28/23, to administer Risperdal oral tablet 0.5 mg by mouth two times a day for paranoid delusions
manifested by false accusation that someone taking her money and sertraline hcl oral tablet 25 mg by
mouth one time a day for depression manifested by sadness.
Review of the Order Summary Report for January 2024 showed the order for Risperdal 0.5 mg was
changed on 1/4/24, to be administered one time a day for paranoid delusions manifested by false
accusation that someone taking her money.
Review of Resident 25's care plan dated 12/28/23, showed the resident used Risperdal medication.
However, the care plan failed to show the interventions to monitor for the false accusation behavior and
provide non-pharmacological interventions. In addition Resident 25's care plan failed to show the care plan
problem to address the use of sertraline hcl medication for depression manifested by verbalization of
crying, monitoring for its effect and any adverse drug reactions and non-pharmacological interventions.
On 1/24/24 at 1515 hours, an interview and concurrent record review was conducted with LVN 5. LVN 5
verified the comprehensive care plan for Resident 25 did not include the monitoring of behavior
manifestations related to Resident 25's use of Risperdal, and no care plan problem to address the
resident's depression and use of sertraline hcl.
On 1/24/24 at 1600 hours, an interview and concurrent record review was conducted with the MDS/RAI
Coordinator. The MDS/RAI Coordinator verified Resident 25's comprehensive care plan failed to show the
behavior manifestations related to Resident 25's use of Risperdal and a care plan problem to address for
the resident's depression and use of sertraline hcl.
On 1/25/24 at 1407 hours, an interview was conducted with the DON. The DON stated the comprehensive
care plan should have been developed for Resident 25's use of Risperdal and sertraline hcl. The DON was
informed and acknowledged the above findings.
3. Medical record review for Resident 679 was initiated on 1/23/24. Resident 679 was admitted to the facility
on [DATE], and readmitted on [DATE].
Review of Resident 679's Order Summary Report showed a physician's order dated 1/18/24, to check PVR
Q six hours, perform IN and OUT catheterization (a method of emptying the bladder) Q six Hours PRN if
PVR more than 125 ml or equal, insert Foley catheter on the 3rd check every six hours for bladder training
outcome for two days and notify MD of Outcome.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 10 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Review of Resident 679's Plan of Care failed to show a care plan problem was developed to address the
PVR monitoring as ordered by the physician.
On 1/25/24 at 0755 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 acknowledged Resident 679's Plan of Care did not have a care plan problem to address the
physician's order to check for PVR.
Event ID:
Facility ID:
555768
If continuation sheet
Page 11 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0657
Level of Harm - Potential for
minimal harm
Residents Affected - Some
Develop the complete care plan within 7 days of the comprehensive assessment; and prepared, reviewed,
and revised by a team of health professionals.
Based on interview and medical record review, the facility failed to ensure the comprehensive plans of care
for one of 13 final sampled residents (Resident 25) were revised to reflect the residents' current care needs
and interventions.
* The facility failed to revise the comprehensive plan of care for Resident 25's diagnosis of dementia (a
memory impairment and disruption of thought process that impacts a person's ability to perform daily
activities). This posed the risk of not providing the resident with individualized and person-centered care.
Findings:
Medical record review for Resident 25 was initiated on 1/24/24. Resident 25 was admitted tot the facility on
12/28/23, with a diagnosis of dementia.
Review of Resident 25's History and Physical examination dated 12/29/23, showed Resident 25 was
admitted to the facility for dementia and had no capacity to understand and make decisions.
Review of Resident 25's Order Summary Report dated 1/24/24, showed a physician's order dated
12/28/23, to administer donepezil Hcl (medication used to treat dementia) 5 mg one tablet by mouth at
bedtime for dementia.
Review of Resident 25's plan of care showed a care plan problem dated 12/28/23, to address Resident 25's
cognitive function and thought process. However, the interventions did not show specific interventions
including non-pharmacological approaches to support the resident and lessen their distress and the use of
the medication for dementia.
On 1/25/24 at 1036 hours, an interview and concurrent medical record review for Resident 25 was
conducted with RN 1. RN 1 verified Resident 25 had a diagnosis of dementia and on the medication. RN 1
was asked about Resident 25's plan of care for the diagnosis of dementia, RN 1 verified there was a plan of
care for dementia and the interventions did not include the non-pharmacological approaches to lessen the
resident distress and pharmacological interventions used for dementia.
On 1/25/24 at 1613 hours, an interview and concurrent medical record review for Resident 25 was
conducted with the DON. The DON was informed and verified the above findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 12 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
Provide appropriate treatment and care according to orders, resident’s preferences and goals.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and medical record review, the facility failed to provide the services to attain or
maintain the highest practicable well-being for three of 13 final sampled residents (Residents 8, 9, and
679).
Residents Affected - Few
* Resident 9 was administered olmesartan medoxomil (medication to treat high blood pressure) and
metoprolol (medication to treat high blood pressure) when Resident 9's systolic blood pressure was below
the parameter prescribed by the physician.
* The facility failed to continue to monitor and document assessment every shift for 72 hours after the
change in condition identified for Resident 8.
* The facility failed to ensure the physician's orders were followed related to monitoring of Resident 679's
urinary output and PVR.
These failures had the potential to negartively affect the residents' health condition and well-being.
Findings:
1. Medical record review for Resident 9 was initiated on 1/23/24. Resident 9 was admitted to the facility on
[DATE].
Review of Resident 9's Order Summary Report showed the following physician's orders:
- On 10/4/23, to administer metoprolol tartrate 25 mg one tablet by mouth two times a day for hypertension
(high blood pressure. Hold medication if systolic blood pressure less than 130 mmHg, or heart rate less
than 60 beats per minute; and
- On 10/25/23, to administer olmesartan medoxomil 40 mg one tablet by mouth every 48 hours for
hypertension. Hold if systolic blood pressure less than 130 mmHg, or heart rate less than 60 beats per
minute
a. Review of Resident 9's MAR for November 2023 showed Resident 9 was administered the metoprolol
medication when the resident's systolic blood pressure was below 130 mmHg as follows:
- On 11/3/23 at 1700 hours, a blood pressure of 115/54 mmHg;
- On 11/4/23 at 0900 hours, a blood pressure of 119/87 mmHg;
- On 11/6/23 at 1700 hours, a blood pressure of 128/87 mmHg;
- On 11/15/23 at 1700 hours, a blood pressure of 117/67 mmHg;
- On 11/18/23 at 1700 hours, a blood pressure of 128/88 mmHg;
- On 11/19/23 at 0900 hours, a blood pressure of 121/66 mmHg;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 13 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
- On 11/25/23 at 1700 hours, a blood pressure of 118/66 mmHg; and
Level of Harm - Minimal harm
or potential for actual harm
- On 11/26/23 at 0900 hours, a blood pressure of 122/66 mmHg.
Residents Affected - Few
Review of Resident 9's MAR for December 2023 showed Resident 9 was administered the metoprolol
medication when the resident's systolic blood pressure was below 130 mmHg as follows:
- On 12/15/23 at 1700 hours, a blood pressure of 126/69 mmHg;
- On 12/18/23 at 1700 hours, a blood pressure of 126/66 mmHg;
- On 12/19/23 at 1700 hours, a blood pressure of 114/68 mmHg;
- On 12/27/23 at 1700 hours, a blood pressure of 128/75 mmHg; and
- On 12/30/23 at 1700 hours, a blood pressure of 118/62 mmHg.
b. Review of Resident 9's MAR for January 2024 showed Resident 9 was administered the olmesartan
medoximil medication when the resident's systolic blood pressure was below 130 mmHg as follows: 121/66
mmHg on 1/4/24, and 102/69 mmHg on 1/13/24.
On 1/26/24 at 1026 hours, an interview and concurrent medical record review for Resident 9 was
conducted with the DON. The DON verified the metoprolol and olmesartan medoximil medications were
administered to Resident 9 when the resident's systolic was below the parameter prescribed by the
physician. The DON stated the nurses should have held the metoprolol and olmesartan medoximil
medications when Resident 9's systolic blood pressure was below 130 mmHg.
2. Medical record review for Resident 8 was initiated on 1/24/23. Resident 8 was admitted to the facility on
[DATE].
Review of Resident 8's H&P examination dated 10/13/23, showed Resident 8 did not have the capacity to
understand and make her own decisions.
a. Review of Resident 8's eInteract SBAR (Situation, Background, Assessment, Recommendation)
Communication Form dated 12/28/23, showed upon body assessment, Resident 8 was noted to have
yellow discharge from the G-tube site with no odor, afebrile, and non-tachycardic; and the dressing was
changed.
Review of Resident 8's Plan of Care dated 12/29/23, showed a care plan problem for infection of the G-tube
site. The care plan interventions included to monitor/document/report to MD for changes in behavior,
altered mental status, wide variation in cognitive function throughout the day, communication decline,
disorientation, periods of lethargy, restlessness, agitation, and altered sleep.
b. Review of Resident 8's eInteract SBAR Communication form dated 1/16/24, showed Resident 8 had a
body temperature of 100 degrees Fahrenheit.
Review of Resident 8's Plan of Care updated on 1/17/24, showed a care plan problem for UTI. The care
plan interventions included to monitor/document/report to MD as needed for signs and symptoms of UTI:
frequency, urgency, malaise, foul smelling urine, dysuria, fever, nausea and vomiting, flank pain,
supra-pubic pain, hematuria, cloudy urine, altered mental status, loss of appetite, and
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 14 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
behavioral changes.
Level of Harm - Minimal harm
or potential for actual harm
However, review of Resident 8's Change in Condition notes showed documentation of assessment only for
the following dates:
Residents Affected - Few
- 12/29/23, for 7-3 shift
- 12/29/23, for 11-7 shift
- 12/30/23, for 3-11 shift
- 12/31/23, for 3-11 shift
- 1/17/24, for 7-3 shift
- 1/17/24, for 3-11 shift
On 1/24/24 at 1029 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 stated the abnormal vital signs and drainage from the G-tube site were considered a change in a
resident's condition or status. RN 1 stated for a change in condition, the licensed nurse had to initiate a
change in condition note documenting the assessment monitoring every shift for 72 hours. RN 1 verified
there was no documentation of change in condition assessment monitoring for 72 hours for Resident 8's
two change of conditions identified on 12/28/23 and 1/16/24.
On 1/25/24 at 0855 hours, an interview was conducted with the DON. The DON stated when the licensed
nurse identified a change in condition for a resident, the Change in Condition assessment monitoring had
to be initiated every shift for 72 hours. The DON was notified of the missing documentation for the Change
in Condition assessment monitoring for Resident 8. The DON acknowledged the above findings.
3. Review of the facility's P&P titled Fluid Intake and Output Monitoring dated 1/2021 showed the facility
shall record output for the residents with indwelling urinary catheter.
Medical Record Review for Resident 679 was initiated on 1/23/24. Resident 679 was admitted to the facility
on [DATE], and readmitted on [DATE].
Review of the Resident's 679 Order Summary Report showed a physician's order dated 1/17/24, to monitor
the resident's total urinary output in cc every shift.
Review of Resident's 679's MAR for January 2024 showed the following recorded output:
- On 1/20/24, for the day shift, 400 cc,
- On 1/20/24, for the evening shift, 400 cc,
- On 1/20/24, for the night shift, 680 cc,
- On 1/21/24, for the day shift, none was recorded,
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 15 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
- On 1/21/24, for the evening shift, 680 cc,
Level of Harm - Minimal harm
or potential for actual harm
- On 1/21/24, for the night shift, none was recorded,
- On 1/22/24, for the day shift, 600 cc,
Residents Affected - Few
- On 1/22/24, for the evening shift, 400 cc, and
- On 1/22/24, for the night shift, 600 cc.
On 1/25/24 at 0755 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 acknowledged there were missing output documented for the day and on evening shifts on 1/21/24.
b. Review of the Order Summary Report showed a physician's order dated 1/18/24, with start date 1/24/24,
and end date 1/26/24, to check PVR every six hours and perform IN and OUT catheterization every six
hours PRN if PVR more than 125 ml or equal.
However, further review of medical record showed no documented evidence the PVR was monitored as
ordered.
On 1/25/24 at 0755 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 acknowledged there was no record for PVR monitoring as ordered by physician.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 16 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0692
Provide enough food/fluids to maintain a resident's health.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview, medical record review, and facility P&P review, the facility failed to follow the physician's order for
the RD consult for one of 13 final sampled residents (Resident 16).
Residents Affected - Few
* The RD did not review the resident's enteral feeding formula for more concentrated formula as ordered by
the physician on 12/25/23, and failed to conduct the RD consultation for weight loss timely as ordered on
1/4/24, for Resident 16. This failure had the potential for a delay or dietary interventions putting the resident
at risk of further undesirable outcomes.
Findings:
Medical record review for Resident 16 was initiated on 1/23/24. Resident 16 was admitted to the facility on
[DATE].
Review of Resident 16's History and Physical examination dated 12/4/23, showed the resident was unable
to eat food by mouth and received nourishment through their G-tube.
a. Review of Resident 16's MAR for December 2023 showed starting 12/7/23, Resident 16 received
Glucerna 1.2 (an enteral feeding formula) via G-tube to run at 70 ml/hr for 20 hours. The record also
showed to flush Resident 16's G-tube every six hours with 200 ml of water starting 12/6/23, and was
discontinued on 12/25/23.
Review of Resident 16's Physician's Progress Note dated 12/22/23, showed Resident 16 had hyponatremia
(low sodium level in the blood) and the physician would monitor and consider a more dilute G-tube feedings
and fluid restriction.
a. Review of Resident 16's Order Summary Report showed a physician's order dated 12/25/23, for the RD
to review if the resident's enteral formula could be changed to a more concentrated formula.
A Physician's Order Note dated 12/25/23 at 1027 hours, showed RN 1 notified Physician 1 of Resident 16's
laboratory results and received a physician's order to decrease the resident's water flushes and for the RD
to see if Resident 16's enteral formula of Glucerna 1.2 could be changed to a more concentrated formula.
A Physician's Order Note dated 12/25/23 at 1051 hours, showed RN 1 notified the RD of the new order for
the RD to review Resident 16's enteral formula to see if it could be changed to a more concentrated
formula, and of the order to decrease the resident's routine water flushes.
* Further review of the medical record showed no documented evidence the RD had review the resident's
formula for more concentrated formula as ordered by the physician.
On 1/26/24 at 1014 hours, an interview and concurrent record review were conducted with RN 1. RN 1
reviewed Resident 16's medical record and was unable to find where the RD reviewed Resident 16's
enteral formula to see if it could be changed to a more concentrated formula.
On 1/26/24 at 1114 hours, a telephone interview was conducted with RD 2. RD 2 stated she was the owner
of the facility's contracted dietetic consultant service. RD 2 stated when there was a
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 17 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0692
physician's order for a RD consult, the standard of practice was to review the resident within 72 hours.
Level of Harm - Minimal harm
or potential for actual harm
On 1/26/24 at 1238 hours, a telephone interview was conducted with Physician 1. Physician 1 stated on
12/25/23, due to Resident 16's hyponatremia and laboratory results, he ordered for the water flushes to be
decreased and for the RD to review if the resident could be changed to a more concentrated enteral
formula. Physician 1 stated the purpose was to decrease Resident 16's fluid intake without decreasing their
calorie intake. Physician 1 stated he had not received an update on it the RD reviewed if a more
concentrated formula could be use.
Residents Affected - Few
On 1/26/24 at 1335 hours, a telephone interview was conducted with RD 1. RD 1 stated Glucerna 1.5 was
more concentrated than Glucerna 1.2.
b. Review of Resident 16's Order Summary Report showed a physician's order dated 1/4/24, for RD consult
for recent weight loss, for a weight of 142.6 lbs on 12/19/23, and 134.8 lbs on 1/2/24 (a 7.8 pounds weight
loss in two weeks). Another physician's order dated 1/8/24, showed to refer to the RD to change enteral
formula to bolus (to consolidate feedings and administer a larger quantity via a syringe or pump).
Review of Resident 16's Nutrition Progress Note dated 1/10/24, showed the RD reviewed Resident 16's
weight loss and recommended Glucerna 1.2, to give two cans (237 ml per can) bolus feeding TID (three
times a day). The record failed to show the RD reviewed Resident 16's weight loss timely for the consult
ordered on 1/4/24.
On 1/26/24 at 1014 hours, an interview and concurrent record review were conducted with RN 1. RN 1
reviewed Resident 16's medical record and verified an order for a RD consult on 1/4/24. RN 1 stated the
record showed the RD reviewed Resident 16 on 1/10/24, and changed the enteral feeding to bolus
feedings.
On 1/26/24 at 1114 hours, a telephone interview was conducted with RD 2. RD 2 stated when there was a
physician's order for a RD consult, the standard of practice was to review the resident within 72 hours.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 18 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0693
Level of Harm - Minimal harm
or potential for actual harm
Ensure that feeding tubes are not used unless there is a medical reason and the resident agrees; and
provide appropriate care for a resident with a feeding tube.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Medical
record review for Resident 16 was initiated on 1/23/24. Resident 16 was admitted to the facility on [DATE].
Residents Affected - Few
Review of Resident 16's MAR for January 2023, showed a physician's order effective 1/11/24, for an enteral
feeding (formula administered directly to the stomach through a tube) of Glucerna 1.2, to give two cans TID
(three times a day).
On 1/23/24 at 0833 hours, Resident 16 was observed lying in bed. Resident 16's bedside table was
observed to have an opened Glucerna 1.2 ready-to-hang bottle. The bottle was labeled 1500 ml and had
markings on the side from 300 to 1500 ml, in 100 increments. The amount of the formula in the bottle was
at the line marked 500 ml.
Review of the manufacturer's guidance for Glucerna 1.2 showed the following:
- for the 237 ml container, to refrigerate after opening.
- for the ready-to-hang container, the instruction showed failure to follow the instructions for use, increase
the potential for microbial contamination. Administer the formula with a feeding set and avoid touching any
part of the container that comes into contact with the formula.
On 1/23/24 at 1121 hours, an observation of Resident 16 was conducted. The opened Glucerna 1.2 enteral
feeding ready-to-hang bottle was still on the resident's bedside table.
On 1/23/24 at 1123 hours, an interview was conducted with LVN 1. LVN 1 stated Resident 16 had a bolus
enteral feeding. LVN 1 stated the facility did not currently have cans of the Glucerna 1.2 to administer to
Resident 16, so the LVN was using the ready-to-hang bottle. The LVN stated they discarded the bottle daily.
When asked if the bottle was safe at room temperature once opened and left at bedside, the LVN replied
they believed it was because when they administered it with a feeding set, it was good for 24 hours. LVN 1
verified they were not using a closed feeding set to administer the formula, and punctured the bottle top
where the feeding set would be inserted so they could pour it into a cup at each scheduled feeding.
On 1/25/24 at 1125 hours, a telephone interview was conducted with the RD. The RD stated she was
unable to find information to show Glucerna 1.2 in the ready-to-hang bottle was safe at room temperature
when administered as a bolus, and not with a feeding set.
Based on observation, interview, medical record review, and facility P&P review, the facility failed to provide
the necessary enteral tube care and services for two of 13 final samples residents (Residents 16 and 629).
* The facility failed to ensure Resident 629's J-tube placement was verified prior to the administration of
medications.
* Resident 16's enteral formula bottle was left at bedside after being opened.
These failures posed the risk for developing complications related to enteral feeding.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 19 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0693
Findings:
Level of Harm - Minimal harm
or potential for actual harm
Review of the facility's P&P titled Administering Medications through an Enteral Tube revised 11/2018
showed steps in the procedure to verify placement of feeding tube prior to the administration of medication
through enteral tube.
Residents Affected - Few
On 1/23/24 at 1045 hours, an observation of medication administration was conducted with LVN 1. LVN 1
was observed to have instilled 15-20 cc of air through Resident 629's J-tube, without use a stethoscope .
LVN 1 did not verify the placement of the J-tube prior to the administration of medication through the J-tube.
Medical record review for Resident 629 was initiated on 1/23/24. Resident 629 was admitted to the facility
on [DATE].
Review of Resident 629's Order Summary dated 1/24/24 showed a physician's order dated 1/13/24, to
check placement of the J-tube before beginning a feeding and before administering medications.
On 1/23/24 at 1456 hours, an interview was conducted with LVN 1. LVN 1 confirmed she failed to use a
stethoscope to listen to verify J-tube placement.
On 1/25/23 at 1520 hours, an interview was conducted with the DON. The DON stated the tube placement
must be verified prior to the administration of medications. The DON was informed and acknowledged the
above findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 20 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0694
Provide for the safe, appropriate administration of IV fluids for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, medical record review, and facility P&P review, the facility failed to ensure one of 13
final sampled residents (Residents 429) received the appropriate care for peripheral intravenous catheter.
Residents Affected - Few
* The facility failed to ensure Residents 429's IV site was assessed and monitored as per the facility's P&P.
This failure posed the risk for a delay in identify and provide necessary care if the resident developed
complications such as catheter-related infections.
Findings:
Review of the facility's P&P titled Administering Medications by IV Push revised 3/2022 showed
assessment, inspect intravenous catheter site and system for signs of complications.
On 01/23/24 at 0833 hours, an IV medication administration observation with RN 1 was conducted. RN 1
was observed cleansing Resident 429's IV port with alcohol wipes then proceeded with administering
ceftriaxone (an antibiotic) 1 gm via IV pump.
Medical record review for Resident 429 was initiated on 1/23/24. Resident was admitted to the facility on
[DATE].
Review of Resident 429's Order Summary dated 1/17-1/24/23, showed a physician's order dated 1/17/24,
to administer ceftriaxone 1 gm intravenously every 24 hours until 1/24/24.
However, further review of the medical record failed to show documented evidence the resident's IV site
was assessed and monitored for signs of complication as per the facility's P&P.
On 1/25/24 at 1503 hours, an interview was conducted with the DON. The DON acknowledged the above
findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 21 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, medical record review, and facility P&P review, the facility failed to ensure the
respiratory services were provided as ordered for three of 13 final sampled residents (Residents 330, 429,
and 629).
Residents Affected - Few
* The facility failed to ensure Resident 330 received continuous oxygen via nasal cannula as per the
physician's order.
* Resident 429's physician's order for oxygen failed to show if the order was continuous or PRN.
* Resident 629's nasal cannula was found in the floor and physician's order for oxygen failed to show if the
order was continuous or as needed.
These failures had the potential for these residents to not receive appropriate respiratory care and increase
risks of infection.
Findings:
Review of the facility's P&P titled Oxygen Administration revised dated 10/2010 showed to verify there is a
physician's order for this procedure and review the physician's orders of facility protocol for oxygen
administration.
1. On 1/24/24 at 1044 hours, 1/25/24 at 0945 hours, and 1/26/24 at 0935 hours, Resident 330 was
observed sitting in the wheelchair in her room. There was no oxygen provided via nasal cannula to
Resident 330.
Medical record review for Resident 330 was initiated on 1/23/24. Resident 330 was readmitted to the facility
on [DATE].
Review of Resident 330's Order Summary Report showed a physician's order dated 1/12/24, for continuous
oxygen at one to two liters per nasal cannula, and may titrate to maintain oxygen saturation level above
90% every shift.
On 1/26/24 at 0938 hours, an observation of Resident 330 and concurrent interview was conducted with
CNA 4. Resident 330 was observed sitting in the wheelchair in her room. There was no oxygen provided via
nasal cannula to Resident 330. CNA 4 verified Resident 330 did not have any oxygen provided via nasal
cannula.
On 1/26/24 at 0958 hours, an observation of Resident 330 and concurrent interview and medical record
review for Resident 330 was conducted with LVN 6. LVN 6 verified Resident 300 had a physician's order for
continuous oxygen at one to two liters per minute via nasal cannula. LVN 6 verified Resident 330 was not
provided with oxygen via nasal cannula as ordered.
On 1/26/24 at 1008 hours, an interview and concurrent medical record review for Resident 330 was
conducted with the DON. The DON verified the above findings.
2. Review of the facility's P&P titled Oxygen Administration dated 1/1/21, showed to verify if
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 22 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
there is a physician's order for supplemental oxygen
Level of Harm - Minimal harm
or potential for actual harm
Medical record review for Resident 429 was initiated on 1/23/24. Resident 429 was admitted to the facility
on [DATE].
Residents Affected - Few
Review of Resident 429's Order Audit Report dated 1/24/23, showed an order for oxygen at 2 lpm via nasal
canula. The order failed to show if it was a continuous or PRN order.
On 1/23/23 at 0831 hours, Resident 429 was observed lying in bed, on room air (without the use of
supplemental oxygen).
On 1/23/23 at 1223 hours, an interview was conducted with LVN 1 and Resident 429's bedside. LVN 1
verified the resident was on room air. LVN 1 was then pulled up Resident 429's physician's orders for
oxygen and stated the order did not show if it was to be continuous or if it was PRN and the order needed
to be clarified from the physician.
3. Review of the facility's P&P titled Oxygen Administration revised 1/1/21, showed to verify there is a
physician's order for this procedure and review the physician's orders or facility protocol for oxygen
administration.
During the initial tour on 1/23/24 at 0858 hours, Resident 629 was observed in bed, sleeping. Resident
629's family member was in the room. Resident 629 had an oxygen concentrator machine. Resident 629's
nasal cannula was observed on the floor. Resident 629's family member stated Resident 629 was using the
nasal cannula on and off.
Medical record review for Resident 629 was initiated on 1/23/24. Resident 629 was admitted on [DATE],
and readmitted on [DATE].
Review of Resident 629's Order Summary Report showed a physician's order dated 1/12/24, for
administering oxygen at 2-4 liters per minute via nasal cannula to keep oxygen saturation level above 90%.
However the physician's order did not show if the oxygen administration was ordered for continuous or as
needed.
On 1/23/24 at 0915 hours, an observation and concurrent interview and medical record review was
conducted with RN 1 and LVN 1. RN 1 and LVN 1 verified Resident 629's nasal cannula was in the floor. RN
1 checked Resident 629's oxygen saturation level and noted at 91%. LVN 1 stated when she assessed
Resident 629 at 0800 hours, the oxygen saturation level was 93% on room air. RN 1 checked the order for
Resident 629's oxygen and verified the order did not show whether to give the oxygen continuous or as
needed. RN 1 stated the nurses had to verify with the physician if the oxygen administration was continuous
or as needed.
On 1/24/24 at 1015 hours, an interview was conducted with the IP. The IP stated the nasal cannula had to
be in a bag labeled with the resident's name and date when not in use. The IP stated if the nasal cannula
was found on the floor, it had been contaminated and had the potential to cause infection when used by the
resident.
On 1/25/24 at 0855 hours, an interview was conducted with the DON. The DON stated the licensed nurses
were expected to verify the order for oxygen administration with indication to administer continuously or as
needed.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 23 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0700
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Try different approaches before using a bed rail. If a bed rail is needed, the facility must (1) assess a
resident for safety risk; (2) review these risks and benefits with the resident/representative; (3) get informed
consent; and (4) Correctly install and maintain the bed rail.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. On 1/23/24
at 0924 hours, 1/24/24 at 1044 hours, and 1/25/24 at 0945 hours, bilateral assist rails were observed on
Resident 330's bed.
On 1/25/24 at 0932 hours, an interview for Resident 330 was conducted with CNA 5. When asked about
Resident 330's use of the assist rails, CNA 5 stated Resident 330 used the assist rails during turning and
repositioning.
On 1/25/24 at 0945 hours, Resident 330 was observed sitting in the wheelchair in her room. Bilateral assist
rails were observed elevated. When asked about the bilateral assist rails, Resident 330 stated she used the
assist rails for turning and repositioning while in bed.
Medical record review for Resident 330 was initiated on 1/23/24. Resident 330 was admitted to the facility
on [DATE].
Review of Resident 330's History and Physical examination dated 1/15/24, showed Resident 330 did not
have the capacity to understand and make decisions.
Review of Resident 330's Generations Initial Assistive Device Data Collection dated 1/12/24, did not show
any entrapment assessment was conducted related to the use of the assist rails.
Further review of the medical record showed no documented evidence a physician's order was obtained
and a care plan problem was initiated related to the use of side rails for Resident 330.
On 1/25/24 at 0950 hours, an interview and concurrent medical record review for Resident 330 was
conducted with RN 1. When asked about the assist rails, RN 1 verified there was no physician's order
obtained, care plan was not initiated and no entrapment assessment conducted related to the use of assist
rails for Resident 330.
Cross-reference to F909, example #3.
4. On 1/23/24 at 0959 hours, 1/24/24 at 1338 hours, and 1/25/24 at 0905 hours, bilateral assist rails were
observed on Resident 9's bed.
On 1/24/24 at 1338 hours, Resident 9 was observed sitting in the wheelchair in her room. Bilateral assist
rails were observed elevated. When asked about the bilateral assist rails, Resident 9 stated she used the
assist rails when she gets out of bed.
Medical record review for Resident 9 was initiated on 1/23/24. Resident 9 was readmitted to the facility on
[DATE].
Review of Resident 9's MDS dated [DATE], showed Resident 9 had moderate cognitive impairment and
required partial/moderate assistance for bed mobility.
Review of Resident 9's Order Summary Report showed a physician's order dated 10/2/23, for the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 24 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0700
Bilateral Joerns deluxe assist handle rails for better repositioning and transfer while in bed.
Level of Harm - Minimal harm
or potential for actual harm
Review of Resident 9's Generations Initial Assistive Device Data Collection dated 9/27/23, did not show any
entrapment assessment was conducted related to the use of the assist rails.
Residents Affected - Few
Review of Resident 9's plan of care showed a care plan problem dated 9/28/23, to address Resident 9's
use of the assist rails bilaterally to aide with bed mobility. The interventions/tasks included to ensure a valid
consent on chart prior to initiating the assist rails and evaluate the resident's ongoing appropriateness for
use of the assist rails for bed mobility.
Further review of the medical record showed no documented evidence an informed consent was obtained
prior to initiating the use of side rails for Resident 9.
On 1/25/24 at 0931 hours, an interview for Resident 9 was conducted with CNA 5. When asked about
Resident 9's use of the assist rails, CNA 5 stated Resident 9 used the assist rails when getting up from bed
and during turning and repositioning.
On 1/25/24 at 0959 hours, an interview and concurrent medical record review for Resident 9 was
conducted with RN 1. When asked about the consent for assist rails, RN 1 verified there were no consent
obtained and entrapment assessment conducted prior to the use of the assist rails for Resident 9.
Cross reference to F909, example #4.
Based on observation, interview, medical record review, and facility P&P review, the facility failed to
complete the entrapment assessments, obtain the physician's orders, and an informed consents prior to the
use of side rails for five of 13 final sampled residents (Residents 9, 25, 330, 379, and 629). These failures
had the potential to put the residents at risk for serious injuries.
Findings:
Review of the facility's P&P titled Bed Rails, Side Rails dated 4/12/21, showed the resident's assessment
must include an evaluation of the alternatives that were attempted prior to the installation or use of a bed
rail and how these alternatives failed to meet the resident's assessed needs. The resident assessment must
also assess the resident's risk from using bed rails. The resident assessment should assess the resident's
risk of entrapment between the mattress and bed rail or in the bed rail itself. Informed consent from the
resident or resident representative must be obtained after appropriate alternative have been attempted
prior to installation and use of bed rails.
1. On 1/23/24 at 0908 hours, and 1/24/24 at 0858 hours, Resident 25 was observed in bed with the left
upper side rails elevated.
Medical record review for Resident 25 was initiated on 1/24/24. Resident 25 was admitted to the facility on
[DATE].
Review of Resident 25's History and Physical examination dated 12/29/23, showed Resident 25 had no
capacity to understand and make decisions.
Review of Resident 25's MDS dated [DATE], showed Resident 25 required substantial assistance of one
staff for bed mobility and transfer.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 25 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0700
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Review of Resident 25's Order Summary Report for January 2024, showed a physician's order dated
12/28/23, for Joerns deluxe (a assistive device attached to the resident's bedframe to assist with mobility)
assist handle times two for better positioning and transfers.
Review of Resident 25's Generations Initial Assistive Device Data Collection dated 12/28/23, showed the
use of bilateral side rails for bed mobility and transfer purposes.
Further medical record review for Resident 25 did not show documented evidence the informed consent for
the use of the side rails were obtained, initiation of care plan for the use of side rails, and entrapment
assessment prior to the installation of side rails.
On 1/24/24 at 1337 hours, an observation and concurrent interview was conducted with CNA 3. CNA 3
verified Resident 25's bilateral side rails were elevated. CNA 3 stated Resident 25 used the side rails for
pulling herself up in bed.
On 1/25/24 at 1006 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 verified Resident 25 had a physician's order for the use of side rails. RN 1 verified there were no
informed consent obtained, entrapment assessment, and care plan developed prior to installing the side
rails.
On 1/25/24 at 1609 hours, an interview for Resident 25 was conducted the DON. The DON was informed
and verified the findings.
Cross reference to F909, example #1.
2. On 1/24/24 at 0836 hours and 1/25/24 at 0846 hours, an observation and concurrent interview was
conducted with Resident 379. Resident 379 was observed in bed with the upper side rails elevated.
Resident 379 stated he was not able to use the side rails because he was in pain when he moved in bed.
Medical record review for Resident 379 was initiated on 1/24/24. Resident 25 was admitted to the facility on
[DATE].
Review of Resident 379's History and Physical examination dated 1/22/24, showed Resident 379 had the
capacity to understand and make decisions.
Review of Resident 379's Order Summary Report for January 2024 showed a physician's order dated
1/22/24, for Joerns deluxe (a assistive device attached to the resident's bedframe to assist with mobility)
assist handle times two for better positioning and transfers every shift.
Review of Resident 379's Generations Initial Assistive Device Data Collection dated 1/22/24, showed the
use of bilateral side rail for bed mobility and transfers.
Further medical record review for Resident 379 did not show documented evidence the informed consent
for side rails were obtained, initiation of care plan for the use of side rails, and entrapment assessment prior
to the installation of side rails.
On 1/24/24 at 1400 hours, an interview for Resident 379 was conducted with CNA 4. CNA 4 verified
Resident 379's use of the side rails. CNA 4 stated Resident 379 was not able to use the side rails in bed.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 26 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0700
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
On 1/25/24 at 1012 hours, an interview and concurrent medical record review for Resident 379 was
conducted with LVN 4. LVN 4 verified there was a physician's order for Resident 379's use of side rails in
bed. LVN 4 stated Resident 379 was not able to move in bed due to pain.
On 1/25/24 at 1019 hours, an interview and concurrent medical record review for Resident 379 was
conducted with RN 1. RN 1 verified there was a physician's order for the use of the side rails. RN 1 verified
there were no informed consent, entrapment assessment, and care plan developed prior to installing the
side rails.
On 1/25/24 at 1606 hours, an interview for Resident 379 was conducted the DON. The DON was informed
and verified the above findings.
Cross reference to F909, example #2.
5. On 1/26/24 at 0954 hours, an observation was conducted with Resident 629. Resident 629 was in bed
and asleep. Resident 629's bed was observed with bilateral upper side rails elevated.
Medical record review for Resident 629 was initiated on 1/26/24. Resident 629 was admitted to the facility
on [DATE], and readmitted on [DATE].
Review of Resident 629's H&P examination dated 1/14/24, showed Resident 629 had the capacity to
understand and make decisions. The examination also indicated Resident 629 had general weakness.
Review of Resident 629's Generations Initial Assistive Device Data Collection dated 1/12/24, showed the
use of bilateral side rails for bed mobility and transfer purposes.
Further review of Resident 629's medical record failed to show the physician's order and informed consent
were obtained for the use of bilateral side rails.
On 1/26/24 at 1000 hours, an observation and concurrent interview was conducted with LVN 2. LVN 2
verified Resident 629's bilateral side rails were elevated. LVN 2 stated Resident 629 used the side rails for
mobility and turning in bed. LVN 2 stated before the use of side rails, the physician's order and consent
should have been obtained, and the side rail and entrapments assessment should be completed.
On 1/26/24 at 1003 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 stated when Resident 629 was readmitted to the facility, the new physician's order and consent
should have been obtained for the use of side rails. RN 1 verified Resident 629 did not have the physician's
order and consent for the use of side rails.
On 1/26/24 at 1310 hours, an interview and concurrent medical record reviewed was conducted with the
DON. The DON verified Resident 629 did not have the physician's order and consent obtained for the use
of bilateral side rails.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 27 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, medical record review, and facility P&P review, the facility failed to provide the
pharmaceutical services for one of 13 final sampled residents (Resident 629) and one nonsampled resident
(Resident 23) to meet the needs of each resident as evidenced by:
* The facility failed to ensure the medications were administered as ordered to Resident 629.
* The facility failed to ensure the controlled drug, hydrocodone-acetaminophen 10 mg-325 mg tablet,signed
out from the controlled drug record were documented as administered on the MAR for Resident 23
* The facility failed to ensure the disposed medications were destructed and mixed with undesirable
substance or a medication destroyer chemical.
These failures had the potential for poor health outcomes to the residents and controlled medications
diversion.
Findings:
1. On 1/23/24 at 0903 hours, medication administration observation was conducted with LVN 1. LVN 1 was
observed administering one medication via J-Tube to Resident 629. Resident 629 was given 3 ml of
oxycodone (a narcotic analgesic) 5 mg/5 ml.
On 1/23/24 at 1045 hours, medication administration observation was conducted with LVN 1. LVN 1 was
observed administering the following two medications via J-tube to Resident 629:
- Gabapentin (works in the brain to prevent seizures and relieve pain for certain conditions in the nervous
system) 600 mg one tablet.
- iron (a mineral the body needs for growth and development) 65 mg one tablet.
Medical record review for Resident 629 was initiated on 1/23/24. Resident 629 was admitted to the facility
on [DATE].
Review of Resident 629's Order Summary dated for January 2024 showed the following physician's orders:
- on 1/13/24, calcium carbonate antacid oral tablet chewable 500 mg one tablet via J-tube one time a day
for supplement.
- on 1/13/24, Coenzyme Q10-Vitamin E oral tablet chewable 100-300 mg- unit one tablet via J-tube one
time a day for supplement
- on 1/15/24, ferrous sulfate oral tablet 325 (65 mg) one tablet via J-tube one time a day for supplement
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 28 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0755
- on 1/12/24, multivitamin with minerals oral liquid 5 ml via J-tube one time a day for supplement
Level of Harm - Minimal harm
or potential for actual harm
- on 1/15/24, nebivolol hcl oral tablet 10 mg 0.5 tablet via J-tube one time a day for hypertension hold if
systolic blood pressure less than 105 mmHg or heart rate less than 60 bpm
Residents Affected - Few
- on 1/15/24, potassium chloride oral solution 20 meq/15 ml (10%) 7.5 ml via J-tube one time a day for
supplement with four to eight ounces of water to prevent gastric irritation
- on 1/13/24, PreserVision Areds two capsules via J-tube for supplement
- on 1/13/24, calcium-cholecalciferol oral tablet 500-5 mg-mcg one tablet via J-tube two times a day for
supplement
- on 1/15/24, docusate sodium oral tablet 100 mg one tablet via J-tube two times a day for bowel
management
- on 1/15/24, dorzolamide hcl ophthalmic solution 2% instill one drop in both eyes two times a day for eye
maintenance wait five minutes between each drop to prevent wash out of previous eye drop
- on 1/15/24, Timolol Maleate Ophthalmic Solution 0.5 % instill one drop in both eyes two times a day for
eye maintenance wait for five minutes between each drop to prevent wash out of previous eye drop - not
given - lunch time
- on 1/13/24, gabapentin oral tablet 600 mg one tablet via J-tube three times a day for pain management
- on 1/22/24, oxycodone hcl oral solution 5 mg/5 ml 3 ml via J-tube every four hours for pain moderate to
severe pain. Give 3 ml via J- tube every four hours as needed for moderate to serve pain
- on 1/15/24, benazepril hcl oral tablet 10 mg four tablets via J-tube one time a day for hypertension. Hold if
systolic blood pressure less than 105 mmHg or heart rate less than 60 bpm
On 1/23/24 at 1456 hours, an interview and concurrent record review was conducted with LVN 1. LVN 1
stated she had given some of Resident 629's medication at 0730 hours, prior to the observation of
medication administration at 1045 hours, because the resident did not want to take all medications at the
same time. LVN 1 was asked to show the medications given at 0730 hours. LVN 1 showed the medication
supply and stated the medications given to Resident 629 were as follows:
- calcium carbonate oral tablet gave ultra strength 1000 mg
- Coenzyme Q10-Vitamin E 10 ml
- multivitamin with mineral one tablet
- PreserVision AREDS two chewable tablets
- potassium chloride oral solution 20 meq/15 ml
- calcium 600 mg tablet
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 29 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0755
- vitamin D 25 mcg (1000 unit) one tablet
Level of Harm - Minimal harm
or potential for actual harm
- docusate sodium oral 100 mg one tablet
- dorzolamide hcl ophthalmic solution 2 % one drop in both eyes was given before lunch time
Residents Affected - Few
- timolol maleate ophthalmic solution 0.5 % instill one drop in both eyes given before lunch time
- benazepril hcl oral tablet 10 mg four tablets (was not given due to blood pressure reading was 104/65
mmHg)
- nebivolol hcl Oral Tablet 10 mg (Nebivolol HCl) 0.5 tablet (was not given due to blood pressure reading
was 104/65 mmHg)
LVN 1 verified Resident 629 were given the following medications via J-tube which were not according to
the physician's orders:
- calcium carbonate oral tablet gave ultra strength 1000 mg was given instead of 500 mg
- multivitamin with minerals tablet was given instead of liquid form
- calcium 600 mg was given instead of 500 mg
- Coenzyme Q10-Vitamin E 10 ml liquid instead of oral chewable tablet form
- PreserVision AREDS capsule was given instead of chewable tablets
On 1/25/24 at 1503 hours, an interview and concurrent medical record review was conducted with the
DON. The DON was informed and acknowledged the above findings.
2. On 1/24/24 at 1050 hours, review of Resident 23's hydrocodone-acetaminophen 10 mg-325 mg tablet
Controlled or Antibiotic Drug Record showed one tablet was taken on the following dates and times:
- 1/4/24 at 1430 hours;
- 1/12/24 at 1800 hours; and
- 1/21/24 at 1700 hours
However, review of Resident 23's MAR for January 2023 showed the above hydrocodone-acetaminophen
10 mg-325 mg tablet removed from the controlled drug record were not documented as administered.
On 1/24/24 at 1050 hours, an interview and concurrent medical record review was conducted with LVN 3.
LVN 3 verified the above findings.
On 1/25/24 at 1510 hours, an interview was conducted with the DON. The DON stated the licensed nurses
were expected to sign out the narcotic medication and document the administration of the narcotic
medication in the MAR after the medication was given to the resident. The DON was informed and
acknowledged findings.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 30 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
3. Review of facility's P&P titled Discarding and Destroying Medications revised November 2022 showed
non controlled and schedule V (nonhazardous) controlled substances are disposed of in accordance with
the state regulations and federal guidelines regarding disposition of non-hazardous medications. For
unused non-hazardous controlled substances that are not disposed by an authorized collector, the
Environmental Protection Agency (EPA) recommends destruction and disposal of the substance with other
solid waste following the steps below:
a. Take the medication out of the original containers.
b. Mix medication, either liquid or solid, with an undesirable substance. Undesirable substances include
sand, coffee grounds, kitty litter, or other absorbent materials. Place the mixture in the sealable bag, empty
can, or other container to prevent leakage.
On 1/24/24 at 0924 hours, a concurrent observation and interview was conducted with the DON. A white
bin with about one-third full of medications was observed with whole tablets and capsules accessible inside
the medication room. The DON stated these medications were disposed and should have the drug
destroyer chemical poured into the bin. The DON poured three half gallon bottles of a drug destroyer
chemical and poured some water right away.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 31 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Implement gradual dose reductions(GDR) and non-pharmacological interventions, unless contraindicated,
prior to initiating or instead of continuing psychotropic medication; and PRN orders for psychotropic
medications are only used when the medication is necessary and PRN use is limited.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview, medical record review, and facility P&P review, the facility failed to ensure one of 13 final sampled
residents (Resident 25) was provided the management for the use of psychotropic medications
(medications that affect the mind, emotions, and behavior).
* The facility failed to ensure non-pharmacological approaches to care were provided for Resident 25 while
receiving risperidone (Risperdal, a medicine that helps with symptoms of some mental health conditions
where someone may see, hear, or feel things that are not there or believe things that are not true or you
feel unusually suspicious) and sertraline (Zoloft, a medication used to treat depression). This failure had the
potential to cause harm to Resident 25.
Findings:
Review of facility's P&P titled Use of Psychotropic Medication dated 5/23/23, showed the residents who use
psychotropic drugs shall receive non-pharmacological interventions to facilitate reduction or discontinuation
of the psychotropic drugs.
Medical record review for Resident 25 was initiated on 1/24/24. Resident 25 was admitted to the facility on
[DATE].
Review of Resident 25's Order Summary Report for December 2023 showed a physician's order dated
12/28/23, to administer Risperdal oral tablet 0.5 mg by mouth two times a day for paranoid delusions
manifested by false accusation that someone taking her money and sertraline hcl oral tablet 25 mg by
mouth one time a day for depression manifested by sadness.
Review of the Order Summary Report for January 2024 showed the order for Risperdal was changed on
1/4/24, to Risperdal oral tablet 0.5 mg by mouth one time a day for paranoid delusions manifested by false
accusation that someone taking her money.
Review of Resident 25's MAR for December 2023 and January 2024 showed Resident 25 had received
Risperdal and sertraline hcl daily since admission. There was no documented evidence of
non-pharmacological interventions provided for the resident.
Further review of Resident 25's care plan problem addressing the use of Risperdal and sertaline hcl
medications failed to show documentation of interventions for non-pharmacological implementation for the
use of the above medications.
On 1/24/24 at 1458 hours, a concurrent observation and interview with Resident 25 was conducted.
Resident 25 was lying in bed. Resident 25 denied sadness and stated she felt fearful at times.
On 1/25/24 at 0922 hours, a concurrent interview and medical record review was conducted with the DON.
The DON stated the residents on psychotropic medications should be provided with non-pharmacologic
interventions and should be documented in the MAR.
Further review of Resident 25's MAR failed to show non-pharmacologic interventions provided for the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 32 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0758
use of Risperdal and sertraline hcl.
Level of Harm - Minimal harm
or potential for actual harm
On 1/25/24 at 1407 hours, an interview conducted with the DON. The DON was informed and
acknowledged above findings.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 33 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
Ensure medication error rates are not 5 percent or greater.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, medical record review, and facility document review, the facility failed to ensure the
medication error rate was below 5%. The facility's medication rate was 18.52%. Two of two licensed nurses
(LVNs 1 and 3) observed administering the medications was found to have errors while administering the
medications to four nonsampled residents (Resident 14, 17, 23, and 630).
Residents Affected - Few
* The facility failed to ensure Resident 17 received the prescribed eye drops in accordance with the facility's
P&P.
* The facility failed to ensure Resident 14's inhalation medication was administered in accordance with the
facility's P&P.
*The facility failed to ensure Resident 25's hydroxychloroquine (a medication used to treat discoid lupus
erythematosus (a chronic inflammatory condition of the skin) was given with food or meal.
* The facility failed to ensure Resident 630's blood pressure was obtained just before giving the medications
to control the blood pressure.
* The facility failed to ensure Resident 630's Peridex (oral rinse for use between dental visits as part of a
professional program for the treatment of gingivitis- inflammation of the gums) mouth or throat solution was
given as prescribed by the physician.
These failures had the potential for the residents developing complications and ineffective therapeutic
effects of the medications.
Findings:
1. Review of the facility's P&P titled Instillation of Eye Drops dated 1/2014 showed steps in the procedure to
gently pull the lower eyelid down, instruct resident to look up. Drop the medication into the mid lower eyelid.
(Note do not touch the eye or eyelid with the dropper). Recap the medication bottle. Instruct the resident to
slowly close his/her eyelids to allow for even distribution of the drops.
Medical record review for Resident 17 was initiated on 1/23/24. Resident 17 was admitted to the facility on
[DATE].
On 01/23/24 at 0930 hours, a medication administration observation was conducted with LVN 3. LVN 3
administered one drop of dorzolamide hcl and timolol malate (eye drops used to treat increased pressure in
the eye caused by glaucoma) ophthalmic solution directly on Resident 17's both eyes. LVN 3 did not pull
down the resident's lower eyelid as per the facility's P&P.
Review or Resident 17's Order Summary Report for 1/2024 showed a physician's order dated 12/28/23, for
dorzolamide hcl and timolol malate ophthalmic solution 0.5%, instill 1 drop in both eyes two times a day for
increased eye pressure.
On 1/23/24 at 1513 hours, an interview was conducted with LVN 3. LVN 3 stated she instilled one drop of
dorzolamide hcl and timolol malate ophthalmic solution 0.5% to Resident 17's both eyes;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 34 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
however, failed to pull down the lower eyelids.
Level of Harm - Minimal harm
or potential for actual harm
On 01/25/23 at 1503 hours, an interview was conducted with the DON. The DON was informed and
acknowledged the above findings.
Residents Affected - Few
2. Review of the facility's P&P titled Administering Medication through a Metered Dose Inhaler revised
10/2010, showed steps in the procedure ask the resident to inhale and exhale deeply for few breath cycles.
On the last cycle, instruct the resident to exhale deeply then place the mouthpiece in the mouth and instruct
the resident to close his or her lips to form a seal around the mouthpiece. Firmly depress the mouthpiece
against the medication canister to administer medication. Instruct the resident to inhale deeply and hold for
several seconds. Remove the mouthpiece from the mouth and instruct the resident to exhale slowly though
pursed lips. Repeat the inhalation, if ordered. Allow at least one minute between inhalations of the same
medications and at least two minutes between inhalations of different medications.
Medical record review for Resident 14 was initiated on 1/23/24. Resident was admitted to the facility on
[DATE].
Review or Resident 14's Order Summary Report for 1/2024 showed a physician's order dated12/28/23, for
Breztri Aerosphere Inhalation Aerosol (a medication used long term to treat people with COPD. It improves
symptoms of COPD for better breathing and to reduce the number of flare-ups) 160 mg - 9 mcg - 4.8 per
inhalation, give 2 inhalations orally two times a day for COPD, and to rinse mouth with water after use.
On 01/23/24 at 0933 hours, a medication observation was conducted with LVN 3. LVN 3 administered two
inhalations of Breztri Aerosphere Inhalation Aerosol 160 mg - 9 mcg - 4.8 per inhalation to Resident 14.
Upon administration of the Breztri Aerosphere Inhalation, LVN 3 placed the mouthpiece of the medication to
Resident 14's mouth. LVN 3 counted one to three then administered the first inhalation to Resident 14.
Resident 14 was not observed to take breaths and to inhale deeply upon administration of the medication.
LVN 3 removed the Breztri Aerosphere Inhalation from Resident 14's mouth. LVN 3 then proceeded to
place the Breztri Aerosphere Inhalation mouthpiece back to Resident 14's mouth again for the second
inhalation. LVN 3 counted one to three. Resident 14 was not observed to take cycle of breaths and did not
inhale deeply as medication was being administered. Right after the Breztri Aerosphere Inhalation
mouthpiece was removed from the Resident 14's mouth, the resident started talking. LVN 3 failed to provide
instructions to the resident to inhale and exhale deeply for few breath cycles prior to the administration of
the medication. Resident 14 was not observed to hold breaths and exhale slowly with pursed lips after
receiving the inhalation. Resident 14 talked right after the mouthpiece was removed from Resident 14's
mouth. LVN 3 did not allow at least one minute in between inhalations of the medication.
On 01/23/24 at 1513 hours, an interview was conducted with LVN 3. LVN 3 stated she was not able to give
instructions to Resident 14 to take deep breaths. LVN 3 stated she usually gave time prior to the
administration of the second inhalation. However, LVN 3 was not able to wait during the medication
administration. LVN 3 verified Resident 14 talked right after the second inhalation was administered.
On 01/25/23 at 1503, an interview with the DON was conducted. The DON was informed and
acknowledged the above findings.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 35 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
Level of Harm - Minimal harm
or potential for actual harm
3. According to Lexicomp by Wolters and Kluwer, provides evidence-based drug information for clinicians
and patients with complex conditions, hydroxychloroquine or systemic lupus erythematosus (an
autoimmune disease in which the immune system attacks healthy parts of the body such as joints, skin,
blood vessels, and organs) and rheumatoid arthritis.) must be administered with food or milk. Do not crush
or divide film-coated tablets per the manufacturer.
Residents Affected - Few
Medical record review for Resident 23 was initiated on 1/23/24. Resident 23 was admitted to the facility on
[DATE].
Review of Resident 23's Order Summary Report for 1/2024 showed a physician's order dated 1/22/24, to
administer hydroxychloroquine 200 mg one tablet by mouth two times a day.
On 1/23/24 at 0956 hours, a medication administration observation was conducted with LVN 3. LVN 3 was
observed administering hydroxychloroquine 200 mg one tablet to Resident 23. Resident 23 did not have
food or meal upon administration of the medication.
On 1/23/24 at 1513 hours, an interview was conducted with LVN 3. LVN 3 stated Resident 23 had breakfast
at 0800 hours. LVN 3 acknowledged the hydroxychloroquine 200 mg one tablet was not administered with
food or meal in accordance to the medication label.
On 01/25/23 at 1503 hours, an interview was conducted with the DON. The DON was informed and
acknowledged above findings.
4. Medical record review for Resident 630 was initiated on 1/23/24. Resident was admitted to the facility on
[DATE].
Review of Resident 630's Order Summary dated for 1/2024 showed the following physician's orders dated:
- 1/20/24, for amlodipine besylate (a medication used for treatment of hypertension) oral tablet 10 mg, give
one tablet by mouth one time a day. Hold for SBP less than 105 mmHg.
-1/20/24, for hydralazine hcl (a medication used for treatment of hypertension.) oral tablet 25 mg, give one
tablet by mouth three time a day. Hold for SBP less than 105 mmHg.
On 1/23/24 at 1019 hours, a medication administration observation and concurrent interview was
conducted with LVN 1. LVN 1 was observed administering amlodipine besylate 10 mg one tablet and
hydralazine hcl oral tablet 25 mg to Resident 630. LVN 1 stated Resident 630's BP was 116/88 mmHg at
0730 hours. LVN 1 further stated she usually took the residents' vital signs in the morning before she
started passing medications.
Further review of Resident 630's MAR showed a blood pressure of 116/88 mmHg was documented on
1/23/24 at 0900.
On 01/25/23 at 1503, an interview with the DON was conducted. The DON was asked regarding procedure
of taking blood pressure for medications with the prescribed parameters for blood pressure. The DON
stated the blood pressure and heart rate should be taken just before giving the prescribed medication. The
DON was informed and acknowledged above findings.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 36 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
5. Medical record review for Resident 630 was initiated on 1/23/24. Resident 630 was admitted to the facility
on [DATE].
On 1/23/24 at 1019 hours, a medication administration observation was conducted with LVN 1. LVN 1
verified Resident 630 would be given 12 tablets/capsules of 10 different medications. LVN 1 was observed
to have given the following medications:
- Aspirin Enteric Coated 81 mg one tablet
- Ubiquinol 100 mg one soft gel
- docusate sodium 100 mg one soft gel
- levetiracetam 500 mg two tablets
- amlodipine besylate 10 mg one tablet
- Vitamin D 25 mg (1000 IU) one tablet
- allopurinol 100 mg one tablet
- acetaminophen 325 mg two tablets
- rosuvastatin calcium 20 mg one tablet
- hydralazine hcl 25 mg one tablet
A medication reconciliation review, post medication administration observation, was conducted for Resident
630. Resident 630 had a physician's order dated 1/20/24, for Peridex mouth/throat solution 0.12 % give 15
ml by mouth every 12 hours for oral care swish and spit out. The Peridex was not administered during the
medication administration observation with LVN 1.
On 1/23/24 at 1456 hours, an interview and concurrent medical record review was conducted with LVN 1.
LVN 1 verified she did not administer the Peridex mouth or throat solution as ordered by the physician.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 37 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
Based on observation, interview, and facility P&P review, the facility failed to ensure the medications were
properly stored and labeled.
* The facility failed to ensure the discontinued medication was locked and not left unattended on top of the
medication cart.
* The facility failed to monitor the temperature of the resident's refrigerator in the medication room.
* The facility failed to appropriately label multiple ointments with open date, dispose of the prescription
ointments such as triamcinolone and mupirocin, dispose of the expired solutions, and maintain cleanliness
of the treatment cart.
* The facility failed to dispose opened sterile packages for IV therapy such as IV holder or lock and
transparent dressing from the IV cart.
* The facility failed to appropriately label the bottle of the iron tablets (supplement) and eye medication
drops with open date.
* The facility failed to dispose of the insulin pen beyond the used by date.
* The facility failed to store the external and internal medications separately.
These failures had the potential to negatively impact the residents' well-being.
Findings:
On 1/23/24 at 1044 hours, a concurrent medication administration observation and interview was
conducted with LVN 1. LVN 1 was observed leaving Resident 29's Baclofen (a muscle relaxant) in a
medication bubble pack card on top of the medication cart unattended and unsecured while passing
medication to another resident. LVN 1 stated the medication was discontinued and was not supposed to be
left on top of the medication cart.
On 1/24/24 at 0808 hours, an inspection of the medication storage and labeling in the medication room and
concurrent interview was conducted with the IP/DSD. The temperature for the freezer for the resident's food
was not being monitored. The IP/DSD stated the freezer temperature should have been monitored.
On 1/24/24 at 0829 hours, an inspection of the medication storage and labeling of the treatment cart was
conducted with LVN 4 with the following findings verified with LVN 4:
- one opened tube calmoseptine cream with no open date
- two opened bottles of Nu gauze packing strip with open date - house supply - 15 days
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 38 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
- one Dyna wound cleanser spray with no open date and resident name
Level of Harm - Minimal harm
or potential for actual harm
- one opened tube Remedy clinical protect no open date and resident name
- two opened tube Remedy clinical moisturizer with no open date
Residents Affected - Few
- one opened Triad hydophilic wound dressing with no open date and resident name
- one opened tub Aquaphor Healing ointment no open date
- one opened tube cream barrier no open date
- one opened solosite wound gel
- two opened tube antifungal greaseless cream
- three opened tubes of triamcinolone acetate 0.1% with prescription label peeled off
- one opened tube mupirocin 2% with no label
- one opened tube hydrocortisone cream with no open date
- Dakins solution 16 oz had expired on 6/23.
- Hydrogen peroxide 16 oz 3% had expired on 6/23.
- Aerosol foam sanitizer had expired on 10/22
- scattered powder in a bin in the 3rd drawer of the treatment cart
On 1/24/24 at 0859 hours, an inspection of the medication storage and IV cart was conducted with RN 1
with the following findings verified with RN 1:
- one IV holder/lock was opened.
- one opened transparent dressing small in the 3rd IV drawer.
- one opened transparent dressing medium in the 3rd IV drawer.
- one pack of good wipes, 60 wipes, had expired on 4/2023.
On 1/24/24 at 1050 hours, an inspection of the medication storage and Medication Cart 2 was conducted
with LVN 3 with the following findings verified with LVN 3:
- An opened bottle of iron 65 mg tablets (supplement) with no open date.
- An open brimonidine tartrate eye drops (used to treat open-angle glaucoma or high fluid pressure in the
eye) with no open date.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 39 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
- An Insulin Lispro injection 100 units (used for diabetic) labeled with the open date of 12/22/23, past 28
days from the open date
- Liothyroxone (used for hypothyroidism) and progesterone capsules (hormone supplement) were stored
with topical estradiol (use to treat changes in and around the vagina caused by low estrogen levels or
menopause) in a zip lock bag.
On 1/25/23 at 1510 hours, an interview was conducted with the DON. The DON stated the medications
such as ointments, creams, and tablets should have been labeled with an open date. The DON verified the
opened sterile items must not be stored in the IV medication cart. The DON verified the insulin pen was
good only for 28 days after the open date. The DON verified the external and internal medications should
be stored in different areas. The DON was informed and acknowledge the above findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 40 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0802
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide sufficient support personnel to safely and effectively carry out the functions of the food and nutrition
service.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, facility document review, and the facility P&P review, the facility failed to ensure the
kitchen staff had the appropriate skill set to safely perform the daily operation of the Food and Nutrition
Services Department.
* Dietary Aides 1 and 2 were unable to demonstrate the thermometer calibration procedure.
* Dietary Aide 1 used the wrong strip to test the chemical concentration measured in parts per million of
quaternary sanitizing solution used to sanitize food contact surfaces, and to test the chlorine concentration
of the dish machine.
* Dietary Aide 2 was unable to correctly describe how to manually wash dishes.
These failures had the potential to lead to foodborne illnesses in a highly susceptible population of
residents who received food prepared in the kitchen.
Findings:
Review of the facility's Diet Type Report dated 1/24/24, showed 30 of the 34 residents residing in the facility
received foods prepared in the kitchen.
Review of the facility's P&P titled Operation and Sanitation revised date 8/31/18, showed to document the
training of al meployees in the use of kitchen equipment using the Competency Checklists (Forms 711-715
or other designated form) and Dietary Employee Orientation Guide (Form 717 or other designated form).
1. According to the USDA Food Code 2022, 4-502.11(B), Good Repair and Calibration, showed food
temperature measuring devices shall be calibrated in accordance with the manufacturer's specifications as
necessary to ensure their accuracy.
Review of the facility's P&P titled How to Calibrate Thermometers: Bi-metallic Stem and Digital revised
12/12/19, showed the procedure on how to calibrate either a bi-metallic stem or a digital thermometer and
to understand the importance of calibration because it resets the thermometer to read accurately.
Review of the [NAME] Waterproof Digital Thermometer Instruction Manual (undated) showed the digital
thermometers that have a bead type thermistor (a resistance thermometer, or a resistor whose resistance
is dependent on temperature) sensor seldom require a calibration or testing. Nevertheless, it is desirable to
calibrate to a specific temperature.
On 1/24/24 at 1124 hours, during the trayline observation, the dietary staff were asked to perform a
thermometer calibration with the CDM and the Culinary Director present. When asked to do a thermometer
calibration, Dietary Aide 1 did not perform a thermometer calibration but checked the food temperature with
a digital thermometer. Dietary Aide 2 was then asked to perform a thermometer calibration, Dietary Aide 2
answered yes but continued to check the food temperature with a digital thermometer. When asked about
the thermometer calibration, the CDM stated they did not perform calibration of
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 41 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0802
the digital thermometers.
Level of Harm - Minimal harm
or potential for actual harm
2. According to the USDA Food Code 2022, 4-501.116, Warewashing Equipment, Determining Chemical
Sanitizer Concentration, showed the concentration of the sanitizing solution shall be accurately determined
by using a test kit or other device.
Residents Affected - Few
According to the USDA Food Code 2017, 4-301.12, Manual Ware washing, sink compartment
requirements, alternative manual ware washing equipment must provide accomplishment of the application
of cleaners and the removal of soil, removal of any abrasive and removal or dilution of cleaning chemicals
and sanitation.
On 1/24/24 at 1403 hours, an observation and interview were conducted with Dietary Aide 1 and the CDM.
The following was observed:
a. Dietary Aide 1 was asked to demonstrate how to check the sanitizing solution of the dishwasher. Dietary
Aide 1 was observed using a pH strip and dipped the strip into the dish surface on the final rinse.
b. Dietary Aide 1 was then asked to demonstrate how to check the sanitizing solution in the sanitation
bucket. Dietary Aide 1 was observed using the chlorine test strips and dipped the strip into a red bucket
filled with sanitizer. The testing strip color did not change. Dietary Aide 1 repeated the steps and the strip
color still did not change.
The CDM verified Dietary Aide 1 used the wrong test strips to check the sanitizing solution in the red bucket
and dishwasher. The CDM stated the chlorine test strip should be used to check the sanitizing solution of
the dishwasher, and the pH testing strip should be used to check the sanitizing solution in the red bucket.
3. According to the Food Code 2022, 4-301.12, Manual Warewashing, Sink Compartment Requirements,
showed the three-compartment requirement allows for proper execution of the three-step manual
warewashing procedure. If properly used, the three-compartments reduce the change of contaminating the
sanitizing water and therefore diluting the strength and efficacy of the chemical sanitizer that may be used.
Review of the facility's P&P titled How to Clean and Sanitize Pots, Pans, Utensils and Dishes revised
1/17/19, showed the following:
- Fill appropriate temperature water to fill lines. Add appropriate amount of detergent and sanitizer. Test and
record on Pot and Pan Litmus Test Log. Scrape and flush out food particles;
- Wash with detergent (110-120 degrees F). Change water every 30 minutes;
- Rinse (110-120 degrees F). Change water frequently;
- Sanitize. Test with appropriate litmus test paper and leave in sanitizing solution for appropriate contact
time; and
- Air dry. Do not towel. Inspect and store dry.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 42 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0802
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
On 1/24/24 at 1607 hours, an interview was conducted with Dietary Aide 2 and with the CDM present.
Dietary Aide 2 was asked the procedure for manual handwashing in the three-compartment sink. Dietary
Aide 2 stated they soaked the dishware with soap and water, sanitized by dunking it in for a little bit and
then rinsed the dishware with water. When Dietary Aide 2 was asked if he had a training on manually
washing the dishware using the three-compartment sink, Dietary Aide 2 answered he was not really
trained, but it was based on experience.
On 1/24/24 at 1610 hours, an interview was conducted with the CDM. When asked if any trainings were
conducted on performing thermometer calibration, checking the sanitizing solution of the dish machine and
sanitizing buckets, and performing manual dish washing using the three-compartment sink, the CDM stated
these competency skills were part of the dietary staff orientation and competency training. However, the
CDM was not able to show documentation of the orientation and competency trainings.
On 1/25/24 at 1500 hours, an interview was conducted with the Culinary Director. When asked what
trainings were provided to the staff, the Culinary Director stated she conducted the trainings last year in
January, however, she had thrown away the training documentation.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 43 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0803
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure menus must meet the nutritional needs of residents, be prepared in advance, be followed, be
updated, be reviewed by dietician, and meet the needs of the resident.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. On 1/23/24
at 1240 hours, a concurrent meal observation and interview was conducted with Resident 632 in his room.
Resident 632 complained his meal tray was missing some of the food he ordered, and he received a food
he did not order. Resident 632's meal ticket showed cob salad, cucumbers, fruit x3, and ice cream x3
marked off. Resident 632's meal tray was observed with missing cobb salad, cucumbers, fruit x3, and ice
cream x3 and there was a light orange pureed food in a small bowl that was not listed in the meal ticket.
The Culinary Director came to the room and verified there were missing food listed in the meal ticket and
there was a pureed food which was a butterscotch pudding in the tray that was not listed.
Medical record review for Resident 632 was initiated on 1/23/24. Resident 632 was admitted to the facility
on [DATE].
Review of Resident 632's H&P examination dated 12/27/23, showed Resident 632 had the capacity to
understand and make his own decisions.
On 01/25/24 at 0930 hours, an interview was conducted with the Culinary Director who oversaw the
resident menu and meals. The Culinary Director stated the meal tickets were based off the menu she
created for the month. She stated the CNAs met with the residents daily to obtain their meal preferences
and check off the food items on the meal ticket for meals on the following day. If the residents did not want
the food items on the meal ticket, they would choose from the menu. The meal ticket was based on what
the residents said they wanted for their meal. The Culinary Director stated all the food or food substitutions
listed on a resident's meal ticket should be served to ensure the resident received their necessary caloric
intake. The Culinary Director further stated it was necessary to follow the resident's preferences.
Based on observation, interview, and facility document review, the facility failed to ensure the menu and
recipes were followed.
* The recipe for the mixed green salad was not followed when cucumbers were not served with the mixed
green salad.
* The lunch meal ticket for Resident 30 was not followed when she was not served with apple juice.
* Resident 632 was not provided with the food he ordered as listed on the meal ticket, and received a food
he did not order.
These failures had the potential for the residents not receiving adequate nutrition, and appropriate food
texture based on their diet.
Findings:
1. Review of the facility's Diet Type Report dated 1/24/24, showed 25 of the 34 residents residing in the
facility received regular-textured food prepared in the kitchen.
Review of the facility's document titled Daily Spreadsheet dated 1/23/24, showed regular/NAS (no added
salt) diet, CCHO/ NAS (consistent carbohydrate) diet and liberal house renal diet included a
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 44 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0803
serving mixed green salad.
Level of Harm - Minimal harm
or potential for actual harm
Review of the menu list dated 1/23/24, showed mixed green salad with dressing was a combination of fresh
salad greens and sliced cucumbers served with dressing.
Residents Affected - Few
Review of the recipe of the mixed green salad showed cucumbers as one of the ingredients.
On 1/23/24 at 1220 hours, during the dining observation, Resident 9 was observed in her room with her
lunch tray in front of her. The lunch tray included a bowl of salad; however, there were no slices of
cucumbers in the salad. When asked about her salad and if she liked it with cucumbers, Resident 9 asked
why she did not get cucumbers in her salad.
On 1/23/24 at 1226 hours, an inspection of the satellite kitchen was conducted with the Culinary Director.
The Culinary Director verified there were no cucumber slices on the mixed green salad served to the
residents. The Culinary Director stated the food served were from the main kitchen, and the kitchen staff
might have forgotten to add the cucumber slices.
2. On 1/24/24 at 1124 hours, during the trayline observation, a random inspection was conducted on the
lunch trays in the tray cart ready to be served to the residents.
Review of the menu ticket for Resident 30 showed to serve apple juice.
Inspection of the lunch tray for Resident 30 did not show an apple juice was included.
Dietary 1 verified the above findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 45 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0806
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure each resident receives and the facility provides food that accommodates resident allergies,
intolerances, and preferences, as well as appealing options.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, medical record review, and facility document review, the facility failed to ensure the
food preferences were honored for one of 13 final sampled residents (Resident 9).
* Resident 329's tray card showed the resident preferred chef salad and cranberry juice. However, this was
not served to the resident. This had the potential to negatively impact the resident's well-being.
Findings:
On 1/23/24 at 1230 hours, during the dining observation, Resident 329 was observed with a mixed green
salad, ravioli with cream sauce, and steamed spinach on her tray. Resident 329 stated she preferred chef
salad and a cranberry juice as per tray card.
On 1/23/24 at 1235 hours, Dietary Aide 1 verified Resident 329 was not served chef salad and cranberry
juice as per the resident's tray card.
Medical record review for Resident 9 was initiated on 1/23/24. Resident 329 was admitted to the facility on
[DATE].
Review of Resident 9's Selection Sheet dated 1/25/24, showed Resident 329's preferred cranberry juice
and chef salad.
Review of Resident 9's [NAME] 101: Dietary Interview Pre-Screen - V2 dated 1/22/24, showed Resident
329's beverage preferences included cranberry juice and meal preferences for lunch included chef salad.
On 1/23/24 at 1236 hours, a concurrent interview and medical record review was conducted with the
Culinary Director. The Culinary Director stated the dietary staff should have followed the resident's
preferences as stated in the tray card.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 46 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
Level of Harm - Minimal harm
or potential for actual harm
Procure food from sources approved or considered satisfactory and store, prepare, distribute and serve
food in accordance with professional standards.
Based on observation, interview, and facility P&P review, the facility failed to ensure the sanitary
requirements were met in the kitchen as evidenced by:
Residents Affected - Some
* The facility failed to ensure proper hand hygiene were practiced by the dietary staff in the satellite kitchen.
* The facility failed to ensure hair and beard restraint were worn by a non-dietary personnel inside the main
kitchen.
* The facility failed to ensure the meat thawing in the refrigerator in the main kitchen was labeled with the
use-by date, and the date when the meat was pulled from the freezer.
* The facility failed to ensure the proper labeling and dating of the food items in the main kitchen and
satellite kitchen.
* The facility failed to ensure the proper labeling and dating of the foods in refrigerator was in placed for the
residents' food brought in by visitors. In addition, the facility failed to ensure the food items were discarded
after a resident has been discharged .
* The facility failed to ensure the expired food items in the main kitchen were discarded.
* The facility failed to ensure the plates, storage bins for bowls and plates, and heated plate dispenser were
clean.
* The facility failed to ensure the employee personal belongings were not stored in the main kitchen food
preparation area.
* The facility failed to air dry the plate bases before using in the trayline service.
* The facility failed to ensure the quaternary sanitizing strips to check the sanitizing solution for the manual
ware washing and sanitization buckets were not expired.
These failures had the potential to cause foodborne illnesses in a medically vulnerable resident population
who consumed food prepared from the kitchen.
Findings:
Review of the facility's Diet Type Report dated 1/24/24, showed 30 of the 34 residents residing in the facility
received foods prepared in the kitchen.
1. According to the USDA Food Code 2022, 2-301, When to Wash, showed food employees shall clean
their hands and exposed portions of their arms immediately before engaging in food preparation, including
working with exposed food, clean equipment, and utensils, and unwrapped single-service and single use
articles; after handling soiled equipment or utensils; during food preparation, as often as necessary to
remove soil and contamination and to prevent cross contamination when changing tasks; before donning
gloves to initiate a task that involves working with food; and after engaging in other
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 47 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
activities that contaminate the hands.
Level of Harm - Minimal harm
or potential for actual harm
Review of the facility's P&P titled Personal Hygiene/ Safety/ Food Handling/ Infection Control revised
5/18/23, under Clean Hand, Fingernails and Gloves section, showed hands must always be washed prior to
beginning work.
Residents Affected - Some
On 1/23/24 at 0810 hours, during the initial inspection of the satellite kitchen, the kitchen sink was observed
not working. A brown stain was observed from the controls to the basin of the kitchen sink. Two dietary staff
in the satellite kitchen were observed wearing disposable food prep gloves and preparing breakfast trays.
Dietary Aide 1 verified the kitchen sink in the satellite kitchen was not working. Dietary Aide 1 stated the
kitchen sink was not working in the morning so they had to use a hand sanitizer and then wear the
disposable food prep gloves.
Cross reference to F908, example # 2.
2. According to the USDA Food Code 2022 Section 2-402.11 Hair Restraints, Effectiveness, showed food
employees shall wear hair restraints such as hats, hair coverings or nets, beard restraints, and clothing that
covers body hair, that are designed and worn to effectively keep their hair from contacting exposed food,
clean equipment, utensils, and linens.
Review of the facility's P&P titled Personal Hygiene/ Safety/Food Handling/ Infection Control revised
5/18/23, under Head Covering Worn section, showed the following:
-Wear a clean hat or other hair restraint. Hair must be appropriately restrained or completely covered;
-Head covering must be clean;
-Beards, mustaches or any body hair that maybe exposed must be covered.
On 1/24/24 at 1120 hours, a technician was observed in the main kitchen. The technician was not wearing
a hair and beard restraints. The Culinary Director verified the findings.
3. According to Food Code 2022, 3-501.13, Thawing, showed freezing prevents microbial growth in foods,
but usually does not destroy all microorganisms. Improper thawing provides an opportunity for surviving
bacteria to grow to harmful numbers and/ or produce toxins.
Review of the facility's P&P titled Refrigerated Storage Chart, under the Meat, Fish, and Poultry - Fresh
section revised 12/28/20, showed the recommended time was at 35 to 41 degrees F or less for beef, lamb,
pork, and veal chops, steaks or roasts is two to four days, while ground meat or stew meat is one to two
days.
On 1/24/24 at 0832 hours, four packs of ground beef with a received date of 1/19/24, and four packs with a
received date of 1/12/24, were observed in the walk-in refrigerator in the main kitchen. There was no date
when the meats were pulled from the freezer. The Culinary Director verified the above findings.
4. Review of the facility's P&P titled Food Receiving and Storage dated 1/1/20, showed the foods stored in
the refrigerator or freezer will be covered, labeled and dated (use by date).
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 48 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
a. On 1/23/24 at 0810 hours, an initial satellite kitchen tour and concurrent interview was conducted with
Dietary Aide 1.
* The following food items were observed in Refrigerator 1:
- Seven clear bowls of cut-up watermelon, cantaloupe and melon, and two Styrofoam bowls of cut-up
peaches were observed on a tray. The bowls of fruits and/or the tray were not labeled with the use-by dates;
- Three cups of orange juice, seven cups of apple juice, and fruit cups were observed on a tray. The cups
and/ or the tray were not labeled with the use-by dates; and
- A container of cut-up peaches was not labeled with the use-by date.
* The following food items were observed in Refrigerator 2:
-One opened gallon milk was not labeled with the opened date and use-by date;
-One opened container of butterscotch pudding was not labeled with the opened date and use-by date;
-One pitcher of iced tea was not labeled with the opened date and use-by date;
-One opened container of salsa was not labeled with the opened date and use-by date; and
-One opened container of prune juice concentrate not labeled with the opened date and use-by date;
Dietary Aide 1 verified the above findings. Dietary Aide 1 stated she forgot to label the food items with the
opened date.
b. On 1/24/24 at 0832 hours, an inspection of the main kitchen and concurrent interview was conducted
with the Culinary Director. The following food items were observed in the dry storage area without the label
of opened date and use-by-date:
- An opened bag of polenta
- An opened bag of egg noodles
- Two opened bags of spaghetti
- An opened bag of tricolor rotini
- Two opened bags of macaroni pasta
- An opened bag of penne rigate pasta
- An opened box of lasagna pasta
- An opened bag of marshmallow
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 49 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
- An opened bag of powdered sugar
Level of Harm - Minimal harm
or potential for actual harm
The Culinary Director verified the above findings.
Residents Affected - Some
5. Review of the facility's P&P titled Food Brought in by Family dated 8/27/21, showed the food brought by
the family/ visitors for individual residents may not be shared with or distributed to other residents. The food
brought by the family/ visitors that left for the resident to consume later will be labeled and stored in a
manner that it is clearly distinguishable from facility-prepared food.
On 1/23/24 at 0834 hours, an inspection of the refrigerator used for residents' food brought in from visitors,
and concurrent interview was conducted with the IP/DSD. The following food items were observed:
- A fruit bowl was not labeled with resident name, room and date received.
- An ice pop was labeled with resident name and room number. The IP/DSD stated the resident had already
been discharged .
- A can of green tea was not labeled with the resident name, room number, and date received.
- A container of vanilla honey yogurt was not labeled with the resident name, room and date received.
The IP/DSD verified the above findings. The IP/DSD stated the food items were supposed to be labeled
with the resident name, room number and date when the food items were received. The IP/DSD stated if
the food item was from the restaurant and/or from home, they were only supposed to keep the food for
three days; but if the food items were store-bought, they could keep the food until consumed or expired, or
give the food back or discard when the resident discharged .
Cross reference to F813.
6. On 1/24/24 at 0832 hours, an inspection of the dry storage in the main kitchen, and concurrent interview
was conducted with the Culinary Director. The following was observed:
-A bag of chocolate chips was observed with a use-by date of 4/28/23;
-A box of small white beans was observed with a use-by date of 11/15/23; and
-A box of small white beans was observed with a use-by date of 4/10/22.
The Culinary Director verified the above findings.
7. According to the USDA Food Code 2022, 4-601.11 Equipment, Food - Contact Surfaces, Nonfood
Contact Surface, and Utensils, the equipment food-contact surfaces and utensils shall be clean to sight and
touch, the food-contact surfaces of cooking equipment and pans shall be kept free of encrusted grease
deposits and other soil accumulations; and the nonfood- contact surface of equipment shall be kept free of
an accumulation of dust, dirt, food residue, and other debris.
According to the USDA Food Code 2017, 4-602.13, Non-Contact Surfaces, nonfood-contact surfaces of
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 50 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
equipment shall be cleaned at a frequency necessary to preclude accumulation of soil residues.
Level of Harm - Minimal harm
or potential for actual harm
On 1/23/24 at 0818 hours, during the initial tour of the satellite kitchen and concurrent interview was
conducted with Dietary Aide 1. The following was observed:
Residents Affected - Some
-The heated plate dispenser was observed with plates inside. The heated plate dispenser was observed
with a brownish stain on the inner panel;
-Five plates on the heated plate dispenser were observed with food debris;
-The storage bin for plates and bowls were observed with food debris; and
-The lids of the storage bins for condiments, and cereals were dirty and dusty.
Dietary Aide 1 verified the above findings.
8. Review of the facility's P&P titled Personal Hygiene/ Safety/ Food Handling/ Infection Control revised date
5/18/23, under the Designated Area for Employee Personal Belongings section showed the following:
- An area in the Director of Food and Nutrition office or dry storage area may be designated as a separate
employee personal belonging area with signage; and
- Personal belongings, beverages and/ or food may be stored in the designated area.
Review of facility's P&P titled Personal Cell Phones dated 9/2020 showed the employees may carry cell
phones on their person while at work, unless explicitly mandated otherwise for any reason by their
supervisor. Cell phone may be used by employees while on scheduled break areas only.
a. On 1/24/24 at 0832 hours, an inspection of the main kitchen and concurrent interview was conducted
with the Culinary Director. The following was observed:
- A cellphone was observed on top of the sink inside the main kitchen; and
- A pen was observed inside the storage bin for flour.
The Culinary Director verified the above findings.
b. On 1/24/24 at 1101 hours, during a follow-up inspection of the main kitchen, a cellphone and a phone
charger were observed in the cereal food preparation area. Dietary Aide 3 verified the above findings.
9. According to the USDA Food Code 2022, 4-901.11, Equipment and Utensils, Air- Drying Required,
showed items must be allowed to drain and to air-dry before being stacked or stored. Stacking wet items
such as pans prevents them from drying and may allow an environment where microorganism can begin to
grow. Cloth drying of equipment and utensils is prohibited to prevent the possible transfer of
microorganisms.
On 1/24/24 at 1120 hours, during the trayline observation, four insulated plate bases were observed
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 51 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
stacked togethe, and ready to be used during the trayline service. The Culinary and CDM verified the above
findings.
10. According to the USDA Food Code 2022, 4-301.12, Manual Ware Washing, the three- compartment
requirement allows for the proper execution of the three-step manual ware washing procedure. If properly
used, the three compartments reduce the chances of contaminating the sanitizing water and therefore
diluting the strength and efficacy of the chemical sanitizer that may be used. Alternative manual ware
washing equipment, allowed under certain circumstances and conditions, must provide for accomplishment
of the same three steps: application of cleaners and the removal of soil, removal of any abrasive and
removal or dilution of cleaning chemicals, and sanitization.
Review of the manufacturer's Safety Information on pH Test Papers (undated) showed the pH test papers
are marked with an expiration date and will perform as designed until that date as long as stored in a dry
area, protected from sunlight.
On 1/24/24 at 1403 hours, an observation and concurrent interview was conducted with Dietary Aide 1.
When asked to check the sanitizer solution of the quaternary sanitizer bucket (red sanitizing bucket),
Dietary Aide 1 was observed checking the concentration of the sanitizer using a piece of quaternary
sanitizer strip. The quaternary sanitizer strip container had an expiration date of 2/1/22. Dietary Aide 1
verified the quaternary sanitizer strip container had expired.
Cross reference to F908, example #1.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 52 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0813
Have a policy regarding use and storage of foods brought to residents by family and other visitors.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and facility P&P review, the facility failed to follow their policy to ensure
foods brought into the facility for residents by visitors were properly stored and safely consumed.
Residents Affected - Few
* The facility failed to ensure the nursing staff were trained on properly labeling the food items brought in by
the visitors for the residents. This failure had the potential for unsafe food handling.
Findings:
Review of the facility's P&P titled Food Brought in by Family dated 8/27/21, showed the following:
- Family members and visitors are requested to inform nursing staff of their desire to bring food into the
facility;
- Nursing staff will provide family/ visitors who wish to bring foods to the facility with a copy of this policy.
Residents will also be provided a copy in a language and format they can understand; and
- All personnel involved in preparing, handling, serving or assisting the resident with meals or snacks will be
trained in safe food handling practices.
On 1/23/24 at 0834 hours, an inspection of the refrigerator used for the residents' food brought in from the
visitors, and concurrent interview was conducted with the IP/DSD. Several food items were observed not
labeled with the resident's name, room and date received. The IP/DSD verified the findings.
On 1/25/24 at 1415 hours, an interview was conducted with the IP/DSD. When asked if the nursing staff
had been educated or trained on the safe storage and handling of resident foods brought in by the visitors,
the IP/DSD stated she had not provided any staff training regarding safe storage and handling of the foods
brought in for the residents by the visitors.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 53 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0814
Dispose of garbage and refuse properly.
Level of Harm - Potential for
minimal harm
Based on observation, interview, and facility P&P review, the facility failed to dispose and store trash in a
sanitary manner.
Residents Affected - Some
* The facility's two of four trash dumpsters' lids were not fully closed. One dumpster lid was fully open and
another dumpster was observed overflowing with garbage, which prevented the dumpster lid to be fully
closed. This failure had the potential to harbor pests.
Findings:
According to the US Food Code 2022 5-501.113, Covering Receptacles, showed receptacles and waste
handling units for refuse, recyclables, and returnable shall be kept covered with tight-fitting lids.
Review of the facility's P&P titled Food-Related Garbage and Refuse Disposal revised 10/2017 showed the
outside dumpsters provided by the garbage pickup services will be kept closed and free of surrounding
litter.
On 1/24/24 at 1348 hours, an observation of trash disposal and concurrent interview with the Plant
Operations Director. The lids of the two of four dumpsters were observed opened. One dumpster lid was
fully open and another dumpster was observed overflowing with garbage, which prevented the dumpster lid
to be fully closed. The Plant Operations Director verified the findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 54 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0842
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Safeguard resident-identifiable information and/or maintain medical records on each resident that are in
accordance with accepted professional standards.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 10. On
1/23/24 at 0924 hours, during the initial tour of the facility, an interview was conducted with Resident 330.
Resident 330 stated she wanted to ask the social worker about her discharge planning.
Medical record review for Resident 330 was initiated on 1/23/24. Resident 330 was readmitted to the facility
on [DATE].
Review of Resident 330's History and Physical examination dated 1/15/24, showed Resident 330 did not
have the capacity to understand and make decisions.
Review of Resident 330's Generations Care Conference - V3 dated 1/13/24, showed the admission care
conference was conducted on 1/16/24 at 1100 hours. Review of the care conference form showed the
sections for medication/ assistive devices, nursing, and social services were blank. Further review of the
care conference form showed only the dietary and vitality personnel were signed, and there were no
signatures from the nursing, therapy, social services, resident, and her responsible party.
On 1/24/24 at 0953 hours, an interview and concurrent medical record review for Resident 330 was
conducted with the SSD. When asked about Resident 330's discharge planning, the SSD stated the
discharge planning was discussed during the care conference conducted with the resident, her responsible
party, and the department heads. The SSD stated the care conference was usually conducted within five
days upon admission, unless the resident or responsible party asked to do it after that. The SSD verified the
care conference form for Resident 330 was incomplete and should have been completed within that
timeframe.
Based on interview, record review and facility P&P, the facility failed to ensure the complete and accurate
medical records for six of 13 final sampled residents (Residents 16, 19, 24, 25, 330, and 430) and one
nonsampled resident (Resident 24).
*Resident 24's insulin was documented incorrectly as being administered in their axilla for 13 instances.
*Resident 16's insulin was documented incorrectly as being administered in their axilla for seven instances.
In addition, Resident 16's Care Conference assessment was not completed timely.
*Resident 25's insulin was documented incorrectly as being administered in their axilla for three instances.
*Resident 19's insulin was documented incorrectly as being administered in their axilla for two instances. In
addition, Resident 19's Care Conference assessment was not completed timely.
*Resident 330's insulin was documented incorrectly as being administered in their axilla for one instance.
*Resident 429's and 430's Care Conference assessments were incomplete.
* Resident 330's Care Conference assessment was not completed timely.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 55 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0842
These failures had the potential for inaccurate and incomplete medical records.
Level of Harm - Minimal harm
or potential for actual harm
Findings:
Residents Affected - Few
1. Medical record review for Resident 24 was initiated on 1/25/24. Resident 24 was admitted to the facility
on [DATE].
Review of Resident 24's MAR for January 2024 showed the following injections of Humalog KwikPen insulin
were administered subcutaneously:
-On 1/1/24 at 1630 hours, 10 units of insulin.
-On 1/1/24 at 2100 hours, 10 units of insulin.
-On 1/2/24 at 1630 hours, 10 units of insulin.
-On 1/2/24 at 2100 hours, 10 units of insulin.
-On 1/3/24 at 2100 hours, 6 units of insulin.
-On 1/5/24 at 1130 hours, 10 units of insulin.
-On 1/5/24 at 1630 hours, 8 units of insulin.
-On 1/6/24 at 1630 hours, 15 units of insulin.
-On 1/6/24 at 2100 hours, 6 units of insulin.
-On 1/12/24 at 1630 hours, 8 units of insulin.
-On 1/14/24 at 1630 hours, 10 units of insulin.
-On 1/15/24 at 0630 hours, 6 units of insulin.
-On 1/18/24 at 1630 hours, 6 units of insulin.
Review of Resident 24's Location of Administration Report for January 2024 showed the above 13 doses
were administered to the resident's axilla.
On 1/25/24 at 1059 hours, an interview was conducted with Resident 24. Resident 24 stated they never
received their insulin in their axilla. The resident stated the nursing staff always injected their insulin into the
back of their upper arms or abdomen.
On 1/25/24 at 1320 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 stated subcutaneous injections were to be administered into the fatty posterior of the arm, abdomen,
or legs, and not the axilla. RN 1 reviewed Resident 24's Medication Administration Record and Location of
Administration Report for January 2024 and verified the insulin was incorrectly documented as
administered to the resident's axilla for 13 doses.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 56 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0842
2. Medical record review for Resident 16 was initiated on 1/23/24. Resident 16 was admitted to the facility
on [DATE].
Level of Harm - Minimal harm
or potential for actual harm
Review of Resident 16's Medication Administration Record for January 2024, showed the following
Residents Affected - Few
injections of Humulin R insulin were administered subcutaneously:
-On 1/1/24 at 2100 hours, 6 units of insulin.
-On 1/3/24 at 2100 hours, 6 units of insulin.
-On 1/14/24 at 0630 hours, 6 units of insulin.
-On 1/14/24 at 1630 hours, 6 units of insulin.
-On 1/14/24 at 2100 hours, 6 units of insulin.
-On 1/15/24 at 0630 hours, 6 units of insulin.
-On 1/18/24 at 1630 hours, 6 units of insulin.
Review of Resident 16's Location of Administration Report for January 2024, showed the above seven
doses were administered to the resident's axilla.
On 1/25/24 at 1320 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 stated subcutaneous injections were to be administered into the fatty posterior of the arm, abdomen,
or legs, and not the axilla. RN 1 reviewed Resident 16's Medication Administration Record and Location of
Administration Report for January 2024, and verified the insulin was incorrectly documented as
administered to the resident's axilla for seven doses.
3. Medical record review for Resident 25 was initiated on 1/25/24. Resident 25 was admitted to the facility
on [DATE].
Review of Resident 25's Medication Administration Record for January 2024, showed on 1/12/24 at 2100
hours, Insulin Glargine 20 units subcutaneously was administered.
Review of Resident 25's Medication Administration Record for January 2024, showed the following
injections of Humulin R insulin were administered subcutaneously:
-On 1/7/24 at 2100 hours, 6 units of insulin.
-On 1/15/24 at 2100 hours, 6 units of insulin.
Review of Resident 25's Location of Administration Report for January 2024, showed the above three
insulin doses were administered to the resident's axilla.
On 1/25/24 at 1320 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 stated subcutaneous injections were to be administered into the fatty posterior of the arm,
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 57 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0842
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
abdomen, or legs, and not the axilla. RN 1 reviewed Resident 25's Medication Administration Record and
Location of Administration Report for January 2024, and verified the insulin was incorrectly documented as
administered to the resident's axilla for three instances.
4. Medical record review for Resident 19 was initiated on 1/23/24. Resident 19 was initially admitted to the
facility on [DATE].
Review of Resident 19's Medication Administration Record for January 2024, showed the following
injections of Insulin Regular Human were administered subcutaneously:
-On 1/3/24 at 1630 hours, 8 units.
-On 1/5 /24 at 1630 hours, 6 units.
Review of Resident 19's Location of Administration Report for January 2024, showed the above two doses
were administered to the resident's axilla.
On 1/25/24 at 1320 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 stated subcutaneous injections were to be administered into the fatty posterior of the arm, abdomen,
or legs, and not the axilla. RN 1 reviewed Resident 19's Medication Administration Record and Location of
Administration Report for January 2024 and verified the insulin was incorrectly documented as
administered to the resident's axilla for two doses.
5. Medical record review for Resident 330 was initiated on 1/25/24. Resident 330 was readmitted to the
facility on [DATE].
Review of Resident 330's Medication Administration Record for January 2024, showed on 1/15/24 at 1630
hours, 6 units of Humalog KwikPen insulin were administered subcutaneously.
Review of Resident 330's Location of Administration Report for January 2024, showed the above dose was
administered to the resident's axilla.
On 1/25/24 at 1320 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 stated subcutaneous injections were to be administered into the fatty posterior of the arm, abdomen,
or legs, and not the axilla. RN 1 reviewed Resident 330's Medication Administration Record and Location of
Administration Report for January 2024 and verified the insulin was incorrectly documented as
administered to the resident's axilla for one dose.
6. Medical record review for Resident 19 was initiated on 1/23/24. Resident 19 was initially admitted to the
facility on [DATE].
Review of Resident 19's Generations Care Conference - V 3 dated 12/10/23, showed Section A was
completed on 1/18/24, and Sections B, C and D were incomplete.
On 1/24/24 at 1015 hours, an interview and concurrent medical record review were conducted with the
SSD. The SSD reviewed Resident 19's Generations Care Conference - V 3 dated 12/10/23, and verified it
was incomplete.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 58 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0842
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
On 1/24/24 at 1420 hours, an interview and concurrent medical record review were conducted with the
DON. The DON stated the Care Conference assessments were available for staff to document in once the
assessment document was created, and the care conference was held within 72 hours after admission.
Review of the assessment screen showed Sections B, C and D were completed on 1/24/24. The DON
reviewed Resident 19's Generations Care Conference - V 3 dated 12/10/23, and verified she had just
competed Sections B, C, and D that day, and they were not completed timely.
7. Medical record review for Resident 16 was initiated on 1/23/24. Resident 16 was admitted to the facility
on [DATE].
Review of Resident 16's Generations Care Conference - V 3 dated 12/4/23, showed Sections A, B, C, and
D were incomplete.
On 1/24/24 at 1420 hours, an interview and concurrent medical record review were conducted with the
DON. The DON stated the Care Conference assessments were available for staff to document in once the
assessment document was created, and the care conference was held within 72 hours after admission.
Review of the assessment screen showed Sections A, B, C and D were completed on 1/24/24. The DON
reviewed Resident 16's Generations Care Conference - V 3 dated 12/4/23, and verified she had just
competed the sections that day, and they were not completed timely.
8. Medical record review for Resident 429 was initiated on 1/23/24. Resident 429 was admitted to the facility
on [DATE].
Review of Resident 429's Generations Care Conference - V 3 dated 1/17/24, showed Sections A, B, C and
D were incomplete.
On 1/24/24 at 1420 hours, an interview and concurrent medical record review were conducted with the
DON. The DON stated the Care Conference assessments were available for staff to document in once the
assessment document was created, and the care conference was held within 72 hours after admission. The
DON reviewed Resident 429's Generations Care Conference - V 3 dated 1/17/24, and verified the
documentation was not completed timely.
9. Medical record review for Resident 430 was initiated on 1/23/24. Resident 430 was admitted to the facility
on [DATE].
Review of Resident 430's Generations Care Conference - V 3 dated 1/17/24, showed Sections A, B, C and
D were incomplete.
On 1/24/24 at 1420 hours, an interview and concurrent medical record review were conducted with the
DON. The DON stated the Care Conference assessments were available for staff to document in once the
assessment document was created, and the care conference was held within 72 hours after admission. The
DON reviewed Resident 430's Generations Care Conference - V 3 dated 1/17/24, and verified the
documentation was not completed timely.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 59 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0867
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Set up an ongoing quality assessment and assurance group to review quality deficiencies and develop
corrective plans of action.
Based on interview and facility document review, the facility failed to implement their POC dated 2/6/23.
There was no documentation to show the facility was monitoring the results of audits to the QAPI
committee meetings to identify if they had achieved compliance threshold of 100% for repeated deficient
practice cited at F695 in accordance with their POC for recertification survey dated 2/6/23. This failure had
the potential to affect the quality of care for all the residents in the facility.
Findings:
On 1/26/24 at 1304 hours, an interview and concurrent facility document review was conducted with the
Administrator and DON. Review of the POC submitted by the facility to the CDPH, L&C Program for the
recertification survey completed on 2/6/23, showed the deficient practice cited at F695 related to oxygen
order not indicating whether the oxygen should be continuous or as needed. The POC included the
following:
* Medical Records, RN Supervisor, the DON and/or designee will monitor daily all oxygen administration
orders.
* Findings will be discussed and reviewed daily during stand-up meeting and at the facility's monthly QAPI
meeting.
* Compliance will be monitored and discussed during daily clinical meeting and at the QAPI meetings with
an expected compliance threshold of 100%.
The Administrator verified the above findings and stated every three months, the QAPI meetings were
conducted to address the POC compliance. The Administrator could not provide documentation on how the
missing reports on the audits for the deficient practice cited at F695 was addressed. The Administrator
stated the facility was not in 100% compliance so they would still be addressing this issue in their quarterly
QAPI meetings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 60 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 8. Review of
facility's P&P titled Laundry Bedding dated 9/1/22, showed the clean linen is protected from dust/ soiling
during transport and storage to ensure cleanliness.
Residents Affected - Few
Review of the facility's P&P titled Personal Cell Phones dated 9/2020 showed employees may carry cell
phones on their person while at work, unless explicitly mandated otherwise for any reason by their
supervisor. Cell phone may be used by employees while on a scheduled break areas only.
On 1/26/24 at 0827 hours, an observation of the laundry area and concurrent interview was conducted with
the Laundry Aide and Plant Operations Director. The following was observed:
a. A cellphone, a container of petroleum jelly, a bag, a purple sweater, a face mask, a faceshield, and
binders were observed on the folding table in the clean area. The binders were observed touching the
resident towels.
b. The laundry P&P were not posted or available in the laundry area.
The Laundry Aide and the Plant Operations Director verified the findings. The Laundry Aide acknowledged
she placed her personal items on the clean folding area. The Laundry Aide stated she was not informed
she could not store her personal items on the clean folding area. When asked about the laundry P&P, the
Laundry Aide and the Plant Ops Director could not locate the P&P, and the Plant Ops Director stated he
would have to print it out.
Based on interview, observation, facility document review, and facility P&P, the facility failed to ensure an
appropriate infection control practices for one of 13 final sampled residents (Resident 429), two
nonsampled residents (Residents 630 and 633) and in the facility laundry service area.
* The facility failed to follow appropriate transmission-based precautions for Resident 429.
* The facility failed to ensure the staff implemented handwashing with soap and water after caring for
Resident 429 who was on contact isolation for C. Difficile to care for another resident.
* The facility failed to ensure equipment used for Resident 429 who was infected with C. Difficle were
appropriately disinfected.
* The bedpans and basins for Residents 630 and 633 in a double bed room were not labelled.
* The facility failed to ensure Resident 679's urinary drainage bag was kept off the floor.
* The facility failed to ensure the employee's personal belongings were not in the clean linen folding area.
These failures had the potential for spread of infections.
Findings:
1. Review of the facility's P&P titled Management of C. Difficile Infections dated 6/25/23, showed
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 61 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Level of Harm - Minimal harm
or potential for actual harm
Clostridioides difficile (C. diff) is a bacterium that causes diarrhea and colitis (inflammation of the colon). It
is spread by direct contact with contaminated objects or the hands of persons who have touched a
contaminated object.
The P&P also showed contact precautions shall be implemented, in addition to the following:
Residents Affected - Few
-All staff are to wear gowns and gloves upon entry into the resident's room and while providing cares.
-Hand hygiene shall be performed by handwashing with soap and water.
-Thoroughly clean and disinfect reusable equipment with sporicidal disinfectant (agent that destroys
bacterial and fungal spores).
Review of the CDC's, Clean Hands Count for Healthcare Providers Factsheet undated, showed C. diff
spores are not killed by alcohol-based hand sanitizer and to wash your hands with soap and water after
removing gloves.
Review of the CDC's, Prevent the Spread of C. diff, reviewed 7/20/21, showed C. diff spores have a
protective coating allowing them to live for months or sometimes years on surfaces.
Medical record review for resident 429 was initiated on 1/23/24. Resident 429 was admitted to the facility on
[DATE].
Review of Resident 429's Order Summary Report dated 1/24/24, showed a physician's order dated
1/17/24, for contact isolation for C. diff.
a. On 1/23/24 at 0831 hours, Resident 429 was observed in bed. Outside the resident's doorway, isolation
signage was posted next to the door above the plastic drawers. On top of the cart, one container of alcohol
based Super Sani-Cloth wipes, one container of Sani-Cloth Bleach wipes, and one pump bottle of
alcohol-based hand sanitizer were observed. Isolation gowns were in the bottom drawer.
On 1/23/24 at 0910 hours, the MDS/RAI Coordinator was observed in Resident 429's wearing a procedure
mask and gloves. No isolation gown was observed in use. The MDS/RAI Coordinator was observed
touching Resident 429's bed controls on the foot of their bed. The MDS/RAI Coordinator removed her
gloves and used alcohol-based hand rub for hand hygiene. The MDS/RAI Coordinator proceeded to the
nurses' station, picked up papers off the copy machine, and walked down another hallway to go speak to a
nurse.
On 1/23/24 at 0913 hours, an interview was conducted with the MDS/RAI Coordinator. The MDS/RAI
Coordinator stated she was doing her routine daily rounds, and greeted Resident 429 and used the
resident's bed controls to adjust their bed. The MDS/RAI Coordinator stated they saw the isolation signage
at the resident's doorway, and that's why they were wearing a procedure mask and gloves. The MDS/RAI
Coordinator verified they used alcohol-based hand rub (ABHR) for hand hygiene and was not wearing an
isolation gown while in the resident's room. When asked what Resident 429 was in isolation for, the
MDS/RAI Coordinator stated she would have to check. When asked what isolation precautions were
needed for C. diff, the MDS/RAI Coordinator stated a gown was also required. When asked if she washed
her hands when leaving the resident's room, the MDS/RAI Coordinator stated they did not have to because
they used ABHR, and was not aware handwashing with soap and water were required for C. diff
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 62 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
isolation precautions.
Level of Harm - Minimal harm
or potential for actual harm
On 1/23/24 at 0917 hours, an interview was conducted with the IP/DSD. The IP/DSD stated for C. diff, the
staff must wear a gown and gloves while in the room. The IP/DSD was not aware the ABHR were not
effective for use with C. diff.
Residents Affected - Few
On 1/23/24 at 0922 hours, and interview was conducted with the Administrator. The Administrator stated for
C. diff, the staff must perform hand washing as ABHR was not effective against C. diff spores.
b. On 1/23/24 at 1144 hours Resident 429's call light indicator was observed being on above the door. CNA
1 donned a gown, gloves, and procedure mask and entered Resident 429's room. The indicator light above
the resident's doorway was turned off. CNA 1 was heard talking briefly to the resident and was observed
removing the gown and gloves, used ABHR, and left the room. CNA 1 stated they knew they were
supposed to wash their hands for C. diff, but they did not touch the resident and just turned off the call light.
c. On 1/23/24 at 1216 hours, the Activity Director was observed in Resident 429's room wearing an
isolation gown, gloves, and procedure mask while talking to the resident. The Activity Director removed the
PPE, and used ABHR, and left the resident's room. The Activity Director verified they used ABHR and did
not wash their hands when leaving the room. The Activity Director stated they brought the resident the Daily
Chronicle (a single sheet paper printout) and turned on the resident's TV. The Activity Director stated they
usually brought the resident crossword puzzles and magazine to read. Sometimes, they would discard the
items when the resident was done with them, or she would wipe down the magazines with the
alcohol-based wipes.
d. On 1/24/24 at 1115 hours, Family Member 1 was observed in Resident 429's room. Family Member 1
was wearing a procedure mask, but was not wearing an isolation gown or gloves. Family Member 1 moved
the resident's bedside tray table, removed a blanket from Resident 429's bed, and placed a blanket just
brought in over the resident.
On 1/24/24 at 1132 hours, LVN 1 was observed in Resident 429's doorway and asked Family Member 1 to
please wear the gown and gloves and to wash their hands when they left. Family Member 1 went to the
doorway and put on an isolation gown and gloves.
On 1/24/24 at 1342 hours, an interview was conducted with Family Member 1. Family Member 1 stated they
were aware Resident 429 was in isolation at the hospital, but today was the first time anyone at the facility
asked them to wear a gown and gloves. Family Member 1 stated they visited Resident 429 daily since their
admission.
5. Review of the facility's P&P titled Clostridium Difficile revised 10/2018 showed steps toward prevention
and early intervention include frequent hand washing with soap and water by staff and residents. When
caring for resident with Clostridioides Difficile Infection (CDI), staff is to maintain vigilant hand hygiene.
Hand washing with soap and water is superior to alcohol based hand rub (ABHR) for mechanical removal
of the clostridium difficile spores.
On 1/23/24 at 0833 hours, an IV medication administration observation was conducted with RN 1. RN 1
used required PPE prior entering Resident 429's room who was on contact isolation. RN 1 programmed the
IV pump in resident's room, cleansed Resident 429's access site, and administered the IV
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 63 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
medication. RN 1 removed PPE after administration of medication by the Resident 429's doorway and
cleansed her hands with alcohol sanitizer. RN 1 then proceeded to prepare IV medication for another
resident (Resident 630).
On 1/23/24 at 1530 hours, an interview was conducted with RN 1. RN 1 stated she did not wash her hands
with soap and water; however, used an alcohol-based sanitizer to clean her hands prior to the preparation
of Resident 630's medications.
On 1/25/24 at 1503 hours, an interview was conducted with the DON. The DON stated the staff were
expected to wash hands with soap and water after caring for a resident who was infected with C. Difficile.
6. Review of the facility's P&P titled Clostridium Difficile revised 10/2018, showed environmental cleaning in
the rooms of resident with Clostridioides Difficile Infection (CDI) is done with a disinfecting agent
recommended for Clostridium Difficile (household bleach and water solution or an Environmental Protection
Agency (EPA) registered germicidal agent effective against Clostridium Difficile spores.
On 1/24/24 at 0859 hours, RN 1 was observed cleaning the IV pole with alcohol sani-wipes from Resident
429 who was on contact isolation for c. difficile because the IV medication was discontinued. RN 1 put
plastic over the IV pole, then stated this was ready for the next resident to use.
On 01/24/24 at 0903 hours, an interview was conducted with RN 1. RN 1 stated she was not aware the
alcohol sani wipes was not sufficient to clean the euipment.
On 1/25/23 at 1503 hours, an interview was conducted with the DON. The DON stated the staff were
expected to know the equipment from a resident infected with CDI should be cleaned with bleach. The DON
was made aware of the above findings and acknowledged the findings.
7. During initial tour of the facility on 1/23/24 at 1159 hours, an observation and concurrent interview was
done with LVN 1 and CNA 2. The bedpans and basins used by Residents 630 and 633 were observed in
the residents' bathroom without a label. LVN 1 and CNA 2 verified the bedpans and basins were not labeled
for Residents 630 and 633. LVN 1 and CNA 2 stated for rooms with two residents, the bedpans and basins
used by residents in the room should have been labeled with their names. When asked who was
responsible to label the equipment, LVN 1 stated either the licensed nurse or the CNA was to label the
equipment during admission.
Medical record review for Resident 630 was initiated on 1/23/24. Resident 630 was admitted to the facility
on [DATE].
Medical record review for Resident 633 was initiated on 1/23/24. Resident 633 was admitted to the facility
on [DATE].
On 1/24/24 at 1015 hours, an interview was conducted with the IP. The IP stated for rooms with two
residents, the bedpans and basins used by the residents should have been labeled with the residents'
names to prevent cross-contamination between the residents. The IP stated the expectation was for either
the licensed nurse or CNA to label the bedpans and basins during the residents' admissions. The IP was
informed and acknowledged the above findings.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 64 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
9. Review of the facility's P&P titled Catheter Care, Urinary revised 8/2022 showed the facility shall ensure
prevention of urinary catheter associated complications, including urinary tract infections, provide resident's
care plan to assess for any special needs of the resident, and ensure the drainage bag are kept off the
floor.
Medical record review for Resident 679 was initiated on 1/23/24. Resident 679 was admitted to the facility
on [DATE], and readmitted on [DATE].
On 1/23/24 at 1238 hours, Resident 679 was observed sitting on his wheelchair, eating his lunch, with the
TV on. Resident 679's indwelling urinary drainage bag was observed laying on the floor.
On 1/23/24 at 1240 hours, an observation and concurrent interview was conducted with LVN 3. LVN 3
verified the indwelling urinary drainage bag was laying on the floor and should be kept off the floor.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 65 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0881
Implement a program that monitors antibiotic use.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview, medical record review, facility document review, and facility P&P review, the facility failed to
monitor and address the use of antibiotic to identify if the resident's condition did or did not meet the
McGeer's criteria (a set of specific definitions to identify true infections in long term nursing facilities) for four
of 12 nonsampled residents (Residents 11, 13, 634, and 635). The facility failed to complete the criteria for
indication of antibiotic use for Residents 11, 13, 634, and 635. In addtion, Resident 13's antibiotic order was
not clarified with the physician regarding the stop date. These failures had the potential to negatively impact
the residents' well-being.
Residents Affected - Few
Findings:
Review of the facility's P&P titled Infection Control 10-Antibiotic Stewardship dated 7/28/23, showed
Infection Preventionist to utilize expertise and data to inform strategies to improve antibiotic use to include
tracking of antibiotics starts, monitoring adherence to evidence-based published criteria during evaluation
and management of treated infections, and reviewing antibiotic resistance patterns in the facility to
understand which infections are caused by resistant organisms. Facility uses CDC's NHSN Surveillance
Definitions, updated McGreer criteria, or other surveillance tool to define infections. Loeb Minimum Criteria
may be used to determine whether to treat infection with antibiotics. All prescriptions for antibiotics shall
specify dose, duration, and indication for use. Antibiotic orders obtained upon admission, whether new
admission or readmission, to the facility shall be reviewed for appropriateness. Antibiotic orders from
consulting, specialty, or emergency providers should be reviewed for appropriateness. New or changed
orders based on antibiotic timeout recommendations will be obtained from the practitioner.
Review of the facility's P&P titled Infection Control 12-Antibiotic Stewardship Surveillance dated 11/15/22,
showed identifying an Infection Preventionist who would review antibiotic utilization as part of the antibiotic
stewardship program identifying specific situations not consistent with appropriate use of antibiotics. At
review conclusion, provider will be notified of review findings as needed.
Review of the facility document was initiated on 1/25/24. The Infection Control Binder containing
Surveillance Data Collection-Infection Control (Urinary Tract Infections for Resident without Indwelling
Catheter) failed to show the criteria to determine for true UTI was completed for Residents 11, 13, 634, and
635. Resident 13's antibiotic order did not show a stop date.
1. Medical record review for Resident 11 was initiated on 1/25/24. Resident 11 was admitted to the facility
on [DATE].
Review of Resident 11's Order Summary Report showed a physician's order dated 12/19/23, for Zosyn
Intravenous Solution 3.375 mg intravenously every eight hours for UTI until 12/25/23 at 2359 hours.
Review of Resident's 11 Surveillance Data Collection-Infection Control (Urinary Tract Infections for Resident
without Indwelling Catheter) dated 12/20/23, showed the criteria checklist to determine if the resident had a
true UTI was not completed.
2. Medical record review for Resident 13 was initiated on 1/25/24. Resident 13 was admitted to the facility
on [DATE] and readmitted on [DATE].
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 66 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0881
Review of Resident 13's Order Summary Report showed the following:
Level of Harm - Minimal harm
or potential for actual harm
a. A physician's order dated 12/18/23, for Cefpodoxime Proxetil oral tablet (antibiotic) give one tablet by
mouth every 12 hours for UTI until 12/23/23 at 2359 hours.
Residents Affected - Few
b. A physician's order dated 12/18/23, for Methenamine Hippurate oral tablet (used to prevent or control
returning urinary tract infections caused by certain bacteria) 1 gm one tablet by mouth one time a day for
UTI prophylaxis.
Review of Resident 13's Surveillance Data Collection-Infection Control (Urinary Tract Infections for Resident
without Indwelling Catheter) dated 12/18/23, showed the criteria checklist to determine if the resident's
infection was true infection or true UTI was not completed.
3. Medical record review for Resident 634 was initiated on 1/25/24. Resident 634 was admitted to the facility
on [DATE].
Review of Resident 634's Order Summary Report showed a physician's order dated 12/13/23, for Bactrim
DS oral tablet 800-160 mg one tablet by mouth one time a day for sepsis until 12/15/23 at 2359 hours.
Review of Resident 634's Surveillance Data Collection-Infection Control (Urinary Tract Infections for
Resident without Indwelling Catheter) dated 12/12/23, showed the criteria checlist to determine if the
resident's infection was true infection or true UTI was not completed.
4. Medical record review for Resident 635 was initiated on 1/25/24. Resident 635 was admitted to the facility
on [DATE].
Review of Resident 635's Order Summary Report showed a physician's order dated 12/1823, for macrobid
Oral Capsule (antibiotic) 100 mg one capsule by mouth two times a day for UTI until 12/18/23 at 2359
hours, and was discontinued on 12/19/23.
Review of Resident 634's Surveillance Data Collection-Infection Control (Urinary Tract Infections for
Resident without Indwelling Catheter) dated 12/12/23, showed the criteria checklist to determine if the
resident's infection was a true infection or true UTI was not completed.
On 1/25/24 at 1321 hours, an interview and concurrent medical record review was conducted with the IP.
The IP stated the criteria to determine for true UTI or true infection should have been completed for the
indication of antibiotics use and the antibiotic order should have a stop date. The IP further stated the
criteria findings should have been communicated with the physician, however, it was not completed. The IP
verified the above findings.
2. Review of the facility's P&P titled Infection Control 12-Antibiotic Stewardship Surveillance dated 11/15/22
showed that all resident antibiotic regimens will be documented via the facility approved antibiotic
surveillance tracking method. Information will include: a) resident name; b) unit number; c) date symptoms
appeared; d) name of antibiotic e)start date of anitibiotic; f) pathogen identified g) site of infection h) date of
culture i) stop date; j) total days of therapy; k) outcome; and l) adverse events.
Medical record review for Resident 13 was initiated on 1/24/24 at 0834 hours. Resident 13 was
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 67 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0881
Level of Harm - Minimal harm
or potential for actual harm
admitted to the facility on [DATE], and readmitted on [DATE]. Resident 13 with diagnosis including UTI, not
specified.
Review of the Order Summary Report showed a physician's order dated 12/24/23, for Methenamine
Hippurate oral tablet 1 gm one tablet by mouth one time a day for UTI prophylaxis.
Residents Affected - Few
On 01/24/24 at 1114 hours conducted interview and concurrent record review with RN 1. RN 1 verified
there was no clarification made with the phycian by the licensed nurses regarding the stop date of the
Methenamine Hippurate ordered on 12/24/23, for UTI prophylaxis for Resident 13.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 68 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0908
Keep all essential equipment working safely.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and facility document review, the facility failed to maintain the essential
kitchen equipment in safe operating condition.
Residents Affected - Some
* The facility failed to ensure the dish machine in the satellite kitchen was working.
* The facility failed to ensure the sink in the main kitchen was not leaking.
* The facility failed to ensure there was no ice buildup and brownish stain in the freezer of the refrigerator
used to store residents' food brought in by the visitors.
These failures had the potential for the equipment to not function in the way it was intended, which could
cause food borne illnesses for the residents.
Findings:
Review of the facility's Diet Type Report dated 1/24/24, showed 30 of the 34 residents residing in the facility
received foods prepared in the kitchen.
According to USDA Food Code 2022, Section 4-501.11, Good Repair and Proper Adjustment, showed the
proper maintenance of equipment to manufacturer specifications helps ensure that it will continue to
operate as designed. Failure to properly maintain equipment could lead to violations of the associated
requirements of the Code that place the health of the consumer at risk.
Review of the Dish Machine Temperature Log - Low Temp for January 2024, showed the instruction as
follows: the dish machine temperatures and chemical levels must be monitored and recorded every meal
period. Wash cycle must be between 110 to 120 degrees F. Chlorine levels must be between 50 to 100 ppm
(parts per million), and quaternary levels must be between 180 to 200 ppm.
Furthe review of the Dish Machine Temperature Log showed the wash temperatures were recorded as
121/124 for breakfast, lunch, and dinner every day from 1/1 to 1/23/24.
1. On 1/24/24 at 1403 hours, an observation of the dish machine and concurrent interview were conducted
with Dietary Aide 1, with the CDM and the Plant Operations Director present. When asked to check the dish
machine water temperature during the wash cycle, Dietary Aide 1 was observed checking the thermometer
gauge which showed 100 degrees F. When asked to demonstrate how to check the sanitizing solution of
the dishwasher, Dietary Aide 1 was initially observed using a pH strip and dipped the strip into the dish
surface on the final rinse. The CDM stated Dietary Aide 1 used the wrong strip and should use the chlorine
strip instead. Dietary Aide 1 was observed using the chlorine test strips and dipped the strip into the dish
surface on the final rinse. The testing strip color did not change. Dietary Aide 1 repeated the steps, and the
strip color still did not change, and the strip only read 10 ppm. The Plant Operations Director and CDM
were observed checking the hoses connected to the bottles of detergent and sanitizer. The Plant
Operations Director and CDM verified the dish machine was not properly dispensing sanitizer.
On 1/24/24 at 1602 hours, a follow-up observation of the dish machine and concurrent interview was
conducted with the CDM. The CDM was observed running the dish machine twice, and the water
temperature was still at 100 degrees F during the wash cycle.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 69 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0908
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
On 1/25/24 at 1050 hours, a follow-up observation of the dish machine and concurrent interview was
conducted Dietary Aide 1. Dietary Aide 1 stated the dish machine was checked by an outside repair vendor
and they had to replace some of the parts of the dish machine.
On 1/25/24 at 1115 hours, an interview was conducted with the Plant Operations Director. The Plant
Operations Director stated he was informed of the outside repair vendor checking the dish machine, to
which he showed the invoice from the outside repair vendor.
Review of the invoice for the dish machine dated 1/25/24, showed, booster heater not reaching
temperature. Unable to get booster heater to reach temperature due to bad heating elements.
2. On 1/24/24 at 0832 hours, an inspection of the main kitchen and concurrent interview was conducted
with the Culinary Director. The sink in the main kitchen was observed continuously leaking from the faucet.
The Culinary Director verified the findings.
On 1/24/24 at 1350 hours, an interview was conducted with the Plant Operations Director. When the Plant
Operations Director was informed of the leaking sink in the main kitchen, the Plant Operations Director
called the Maintenance Assistant to inform him of the leaking sink in the main kitchen. The Maintenance
Assistant stated he already checked and fixed the sink in the main kitchen. A follow-up inspection of the
main kitchen and concurrent interview was conducted with the Plant Operations Director and Maintenance
Assistant. The sink in the main kitchen was still observed leaking from the faucet lever. The Plant
Operations Director and Maintenance Assistant verified the findings.
3. On 1/23/24 at 0834 hours, an inspection of the refrigerator used for the residents' food brought in by the
visitors, and concurrent interview was conducted with the IP/DSD. An ice build-up and a brownish stain was
observed in the freezer of the refrigerator used for residents' food brought in from the visitors. The IP/DSD
verified the findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 70 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0909
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Regularly inspect all bed frames, mattresses, and bed rails (if any) for safety; and all bed rails and
mattresses must attach safely to the bed frame.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. On 1/23/24
at 0924 hours, on 1/24/24 at 1044 hours, and 1/25/24 at 0945 hours, bilateral assist rails were observed on
Resident 330's bed.
On 1/25/24 at 0932 hours, an interview for Resident 330 was conducted with CNA 5. When asked about
Resident 330's use of the assist rails, CNA 5 stated Resident 330 used the assist rails during turning and
repositioning.
On 1/25/24 at 0945 hours, Resident 330 was observed sitting in the wheelchair in her room. Bilateral assist
rails were observed elevated. When asked about the bilateral assist rails, Resident 330 stated she used the
assist rails when for turning and repositioning while in bed.
Medical record review for Resident 330 was initiated on 1/23/24. Resident 330 was admitted to the facility
on [DATE].
Review of Resident 330's medical record did not show an entrapment assessment and bed inspection.
Cross reference to F700, example #3.
4. On 1/23/24 at 0959 hours, on 1/24/24 at 1338 hours, and 1/25/24 at 0905 hours, bilateral assist rails
were observed on Resident 9's bed.
On 1/24/24 at 1338 hours, Resident 9 was observed sitting in the wheelchair in her room. Bilateral assist
rails were observed elevated. When asked about the bilateral assist rails, Resident 9 stated she used the
assist rails when getting out of bed.
On 1/25/24 at 0931 hours, an interview for Resident 9 was conducted with CNA 5. When asked about
Resident 9's use of the assist rails, CNA 5 stated Resident 9 used the assist rails when getting up from
bed, and during turning and repositioning.
Medical record review for Resident 9 was initiated on 1/23/24. Resident 9 was readmitted to the facility on
[DATE].
Review of Resident 9's medical record did not show an entrapment assessment and bed inspection.
On 1/25/24 at 1112 hours, an interview for Residents 9 and 330 was conducted with the Plant Operation
Director. The Plant Operation Director stated he was responsible bed inspection including maintaining,
inspecting, and installing the assist rails. The Plant Operations stated the bed inspections were done
weekly. When asked if he had done the entrapment assessment for the assist rails, the Plant Operations
Director stated he did not do any entrapment assessment as the assist rails were enablers and not bed
rails. When asked if he has any documentation of the weekly bed inspection, the Plant Operations Director
verified there were no record of the weekly bed inspection conducted.
Cross reference to F700, example #4.
Based on observation, interview, medical record review, facility document review, and facility P&P
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 71 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0909
Level of Harm - Minimal harm
or potential for actual harm
review, the facility failed to ensure the residents' bed were inspected, entrapment assessments were
completed, and with the record of the bed inspection when identifying areas of possible entrapment with
the use of bed rails for four of 13 final sampled residents (Residents 9, 25, 330, and 379). These failures
had the potential to negatively impact the residents resulting in possible entrapment, serious injury, and
death.
Residents Affected - Few
Findings:
According to the Hospital Bed System Dimensional and Assessment Guidance to Reduce Entrapment, the
term entrapment describes an event in which a patient/resident is caught, trapped, or entangled in the
space in or about the bed rail, mattress, or hospital bed frame. Patient entrapments may result in deaths
and serious injuries. These entrapment events have occurred in openings within the bed rails, between the
bed rails and mattresses, under bed rails, between split rails, and between the bed rails and head or foot
boards. The population most vulnerable to entrapment are elderly patients and residents, especially those
who are frail, confused, restless, or who have uncontrolled body movement. The seven areas in the bed
system where there is a potential for entrapment are:
- Zone 1: within the rail;
- Zone 2: under the rail, between the rail supports or next to a single rail support;
- Zone 3: between the rail and the mattress;
- Zone 4: under the rail, at the ends of the rail;
- Zone 5: between split bed rails;
- Zone 6: between the end of the rail and the side edge of the head or foot board; and
- Zone 7: between the head or foot board and the mattress end.
Review of the facility's P&P titled Bed Safety dated 9/23/22, showed the inspection of all beds and related
equipment including the frame, mattress, assistive devices, and bed accessories. The assistive devices
were properly installed using the manufacturer instructions and other pertinent safety guidance to ensure
proper fit. There should be an assessment of the resident using assistive device for bed mobility. If side rails
were used, the maintenance staff will inspect the rails monthly and as needed to ensure the rails are in
proper working order and placed appropriately in bed.
1. On 1/23/24 at 0908 hours, and 1/24/24 at 0858 hours, Resident 25 was observed in bed with the left
upper side rails was elevated.
Medical record review for Resident 25 was initiated on 1/24/24. Resident 25 was admitted to the facility on
[DATE].
Cross reference to F700, example #1.
2. On 1/24/24 at 0836 hours and 1/25/24 at 0846 hours, an observation and concurrent interview with
Resident 379. Resident 379 was observed in bed with the upper side rails elevated. Resident 379 stated he
was not able to use the side rail because he was in pain when he moves in bed.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 72 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0909
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Medical record review for Resident 379 was initiated on 1/24/24. Resident 379 was admitted to the facility
on [DATE].
On 1/25/24 at 1112 hours, an interview for Resident 25 and 379 was conducted with the Plant Operation
Director. The Plant Operation Director stated he was responsible for inspecting, fixing, and placing the side
rails in bed weekly and as needed. The Plant Operation Director was asked if the entrapment assessment
was done for the bed rails. The Plant Operation Director stated the entrapment assessment was not done
because the enabler was not considered a bed rails. When asked if there was any record log for the bed
inspection, the Plant Operation Director verified there was no record log of bed inspection and entrapment
assessment.
On 1/24/24 at 1609 hours, an interview was conducted with the DON. The DON was informed and verified
the above findings.
Cross reference to F700, example #2.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 73 of 74
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
555768
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Yorba Linda Post-Acute
17803 Imperial Highway
Yorba Linda, CA 92886
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0925
Make sure there is a pest control program to prevent/deal with mice, insects, or other pests.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, facility document review, and facility P&P review, the facility failed to
maintain the effective pest control program to prevent the presence of gnats in the main kitchen and the
satellite kitchen. This failure had the potential to lead to food-borne illnesses (illnesses caused by food
contaminated with bacteria, viruses, parasites or toxins) to the residents who eat food prepared in the
kitchen.
Residents Affected - Few
Findings:
Review of the facility's Diet Type Report dated 1/24/24, showed 30 of the 34 residents residing in the facility
received foods prepared in the kitchen.
According to the USDA Food Code 2022, 6-501.111 Controlling Pests, showed insects and other pests are
capable of transmitting disease to humans by contaminating food and food-contact surfaces. Effective
measures must be taken to eliminate their presence in food establishments.
Review of the facility's P&P titled Pest Control revised May 2008 showed the facility maintains an ongoing
pest control program to ensure that the building is kept free of insects and rodents.
On 1/24/24 at 0832 hours, an inspection of the main kitchen and concurrent interview was conducted with
the Culinary Director. Gnats were observed in a bag of bread and in the food preparation area in the main
kitchen. The Culinary Director verified the findings. The Culinary Director stated they had a fly trap in the
main kitchen.
On 1/24/24 at 1339 hours, an interview was conducted with the Plant Operations Director. When asked
about the gnats in the kitchen, the Plant Operations Director stated the pest prevention company came last
month, to which he showed the service information.
Review of the service information conducted by the pest control company dated 12/8/23, showed there
were no pest activity during the pest control company inspection to the facility.
On 1/24/24 at 1602 hours, an inspection of the satellite kitchen and concurrent interview was conducted
with the CDM. Gnats were observed in the food preparation area in the main kitchen. The CDM verified the
findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555768
If continuation sheet
Page 74 of 74