F 0557
Level of Harm - Potential for
minimal harm
Residents Affected - Some
Honor the resident's right to be treated with respect and dignity and to retain and use personal
possessions.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and medical record review, the facility failed to ensure the dignity was maintained for
one nonsampled resident (Resident 298) reviewed for urinary catheter care.
* The facility failed to ensure the Resident 298's urinary catheter drainage bag was covered. This failure
created the potential to affect the residents' well-being.
Findings:
Review of the facility's P&P titled Dignity dated 2/2021 showed all the residents should be cared for in a
manner that promotes and enhances his or her sense of wellbeing. Facility staff should promote, maintain
and protect resident privacy, including bodily privacy during assistance with personal care and during
treatment procedures.
On 5/12/25 at 0911 hours, Resident 298 was observed in bed with an uncovered urinary catheter drainage
bag at the side of the bed.
On 5/12/25 at 1038 hours, Resident 298 was observed up in his wheelchair and the uncovered urinary
catheter drainage bag was placed under the wheelchair.
On 5/13/25 at 0942 hours, Resident 298 was again observed in bed with an uncovered urinary catheter
drainage bag at the side of the bed.
Medical record review for Resident 298 was initiated on 5/13/25. Resident 298 was admitted to the facility
on [DATE].
Review of Resident 298's MDS assessment dated [DATE], showed Resident 298 had mild cognitive
impairment. The resident had an indwelling urinary catheter and needed total assistance from the staff for
urinary catheter care.
Review of Resident 298's Order Summary Report dated 5/13/25, showed a physician's order dated
5/11/25, for a urinary catheter care every shift and to change the urinary catheter bag as needed.
Review of Resident 298's care plan for urinary retention dated 5/2/25, showed interventions including
position the urinary catheter bag and tubing below the level of the bladder and away from the entrance
door. However, there no intervention to place the urinary catheter drainage bag in a privacy bag.
(continued on next page)
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 43
Event ID:
555295
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 0557
Level of Harm - Potential for
minimal harm
Residents Affected - Some
On 5/13/25 at 1414 hours, an observation and concurrent interview for Resident 298 was conducted with
CNA 1. CNA 1 stated Resident 298 had a urinary drainage bag and it needed to be measured for the
amount of urine and emptied at the end of her shift. CNA 1 stated she placed the urinary catheter drainage
bag under the wheelchair and at the side of the bed. CNA 1 verified Resident 298's urinary catheter
drainage bag was not covered with a privacy bag. CNA 1 stated the urinary catheter drainage bag should
have been covered with a privacy bag.
On 5/13/25 at 1441 hours, an interview and concurrent medical record review for Resident 298 was
conducted with LVN 2. LVN 2 verified the physician's order for Resident 298's indwelling urinary catheter
connected to the urinary catheter drainage bag. LVN 2 was informed of the observation about Resident
298's urinary catheter drainage bag was not covered with a privacy bag. LVN 2 stated CNA 1 informed her
of Resident 298's urinary catheter drainage bag not covered with a privacy bag. LVN 2 further stated she
provided CNA 1 with a privacy bag and instructed to place it on Resident 298's urinary catheter drainage
bag.
On 5/15/25 at 1045 hours, an interview and concurrent medical record review for Resident 298 was
conducted with the DON. The DON stated she expected the nurses to provide a privacy bag to the
resident's urinary catheter drainage bag to provide dignity to the residents. The DON was informed and
verified the findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 2 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
Residents Affected - Few
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** Based on
interview, medical record review, and facility P&P review, the facility failed to provide written information
regarding the right to formulate advance healthcare directives for one of 13 final sampled residents
(Resident 19) and one nonsampled resident (Resident 298) reviewed for formulation of advance healthcare
directives. This failure had the potential for the residents' decisions regarding their healthcare and treatment
options not being honored.
Findings:
Review of the facility's P&P titled Advanced Directives revised September 2022 showed the following:
- Prior to admission of a resident, the social services director or designee inquires of the resident, his/her
family members and/or his or her legal representative, about the existence of any written advanced
directives.
- The resident or representative is provided with written information concerning the right to accept or refuse
medical or surgical treatment, and to formulate an advanced directive if he or she choose to do so.
- Written information about the right to accept or refuse medical or surgical treatment, and the right to
formulate an advance directive is provided in a manner that is easily understood by the resident or
representative.
- If the resident or representative indicates that he or she had not established advance directives, the facility
staff will offer assistance in establishing advance directives.
- If the resident or the resident representative has executed one or more advance directive(s), or executes
one upon admission, copies of these documents are obtained and maintained in the same section of the
residents medical record and are readily retrievable by any facility staff.
1. Medical record review for Resident 298 was initiated on 5/13/25. Resident 298 was admitted to the facility
on [DATE].
Review of Resident 298's H&P examination dated 4/30/25, showed Resident 298 had the capacity to
exercise the rights and sign necessary documents.
Review of Resident 298's POLST dated 4/30/25, showed under Section D Information and Signatures,
Resident 298 had no advance directive.
Review of Resident 298's Advance Directive Acknowledgment Form dated 4/29/25, showed the box for I
have executed an Advance Directive was checked off. The form showed a signature for the
resident/representative; however, there was no facility staff signature.
Further review of Resident 298's medical record failed to show documented evidence Resident 298 was
provided with the written information regarding advance directives.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 3 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
Residents Affected - Few
On 5/15/25 at 0944 hours, an interview and concurrent medical record review for Resident 298 was
conducted with the Case Manager. The Case Manager stated she was responsible for the gathering of the
advance directives when a resident was admitted to the facility. The Case Manager stated she would ask
the resident or resident's family member if they had a copy and if so, requested a copy of the advance
directive. The Case Manager stated she assisted the residents or family members to formulate the advance
directive and complete the Advance Directive Acknowledgement form if they did not have an advance
directive. The Case Manager stated she remembered talking to Resident 298 and his family member about
the advance directive and Resident 298's family member informed her that Resident 298 had executed an
advance directive. The Case Manager was asked if she requested a copy of Resident 298's advance
directive and if she documented the conversation with Resident 298 and his family member. The Case
Manager reviewed the progress notes and was unable to show documentation about Resident 298's
advance directive. The Case Manager verified and acknowledged the findings.
On 5/15/25 at 1045 hours, an interview and concurrent medical record review for Resident 298 was
conducted with the DON. The DON stated she expected the case manager would complete the advance
directive acknowledgement form for the residents when they admitted to the facility. The DON was informed
and verified the findings.
2. Medical record review for Resident 19 was initiated on 5/12/25. Resident 19 was readmitted to the facility
on [DATE].
Review of Resident 19's MDS assessment dated [DATE], showed Resident 19's BIMS score was zero,
indicating severe cognitive impairment.
Review of Resident 19's POLST, undated, failed to show the completion of section D for advanced directive.
Review of Resident 19's Advance Directive Acknowledgement dated 12/6/24, showed Resident 19 wished
to execute an advance directive.
On 5/12/25 at 1051 hours, an interview and concurrent medical record review for Resident 19 was
conducted with the DSD. The DSD reviewed Resident 19's POLST and verified the incomplete of section D
for Advance Directive.
On 5/14/25 at 1104 hours, an interview and concurrent medical record review for Resident 19 was
conducted with the SSD. The SSD reviewed Resident 19's POLST and verified it did not show completion
of section D for Advance Directive. The SSD stated Resident 19 was not able to execute an advance
directive and offered resources to Family Member 2. The SSD verified there was no documentation of
resources or follow up provided to Family Member 2. The SSD stated there was no advance directive
available in Resident 19's medical record and verified the above findings. The SSD stated the process in
executing an advance directive was initiated by the admitting nurse, and the SSD would follow up the next
day. If the resident did not have an advance directive, the SSD would offer the resident or responsible party
the information on how to obtain conservatorship when the resident was incapable of making medical
decisions. Furthermore, the SSD stated the process and resources provided in executing an advance
directive to the resident and responsible party must be document in the medical record. The SSD stated if it
was not documented, it meant it was not completed.
On 5/15/25 at 1505 hours, an interview was conducted with the DON. The DON was asked the facility's
process in completing the POLST and obtaining the advance directive. The DON stated upon the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 4 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
resident's admit to the facility, the admitting nurse must complete the POLST. The DON further stated the
SSD was responsible to check for completion of the POLST and follow up on the advance directive.
Furthermore, the DON stated any follow up with the resident and responsible party must be documented in
the medical record. The DON and Administrator were informed and acknowledged the above findings.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 5 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 0689
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure that a nursing home area is free from accident hazards and provides adequate supervision to
prevent accidents.
**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 (Resident 34) was free from accident hazards. The facility failed to implement floor
mattress as ordered by the physician as a fall risk precaution for Resident 34. This failure had the potential
for serious injury to the resident.
Findings:
Review of the facility's untitled P&P revised 11/29/22, showed bed safety, for the residents who try to get
out of the bed unsafely when alone should be evaluated for a low bed and floor mat.
On 5/13/25 at 0926 hours, during an observation, Resident 34 was lying in bed and no floor mattress was
placed by the bed. Instead, the floor mattress was leaned against the wall.
Medical record review for Resident 34 was initiated on 5/12/25. Resident 34 was admitted to the facility on
[DATE].
Review of Resident 34's care plan report showed a care plan focus dated 10/11/24, to address a high risk
for falls related to Alzheimer's and dementia with poor safety awareness. The interventions included the
application of floor mattress at bedside for safety.
Review of Resident 34's Quarterly MDS assessment dated [DATE], showed Resident 34 had severe
cognitive impairment. Section GG of the assessment showed Resident 34 had impairment to both upper
and lower extremities.
Review of Resident 34's H&P examination dated 4/10/25, showed Resident 34 had no capacity to exercise
the rights and sign the necessary documents; therefore, the resident's family member would be informed of
the medical condition and/or plan of treatment.
Review of Resident 34's Order Summary Report dated 5/12/25, showed a physician's order dated 2/7/25,
for floor mattress at the bedside for safety.
On 5/13/25 at 1409 hours, an interview was conducted with CNA 7. CNA 7 stated she recalled Resident 34
had attempted to get out of bed and floor mattress was used for safety.
On 5/13/25 at 0936 hours, an observation with a concurrent interview was conducted with LVN 2. LVN 2
verified the above findings and stated Resident 34 had a fall incident in the past and the floor mattress
should be in placed at all times when the resident was in bed.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 6 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 provide the
necessary care and services to maintain the IV access for one nonsampled resident (Resident 299).
Residents Affected - Few
* The facility failed to ensure the PICC line catheter measurements were obtained and documented. In
addition, the facility failed to ensure the PICC line plan of care included the measurements of the length of
the external catheter and arm circumference. These failures had the potential to delay the identification of
IV catheter related complications for Resident 299.
Findings:
Review of the facility's P&P titled Central Venous Catheter Care and Dressing Changes dated 10/2024
showed the dressing of the central venous catheter is routinely changed at least every seven days or as
needed when the dressing becomes damp, loosened or visibly soiled. The licensed nurse would measure
the length of the external central vascular access device with each dressing change or if dislodgement is
suspected then compare with length documented at insertion. Also to measure the arm circumference and
compare to baseline when clinically indicated to assess for possible complications.
Medical record review for Resident 299 was initiated on 5/13/25. Resident 299 was admitted to the facility
on [DATE].
On 5/12/25 at 0939 hours, an observation and concurrent interview was conducted with Resident 299.
Resident 299 was sitting in her wheelchair with a PICC line on her left upper arm. The PICC line had a
transparent dressing dated 5/5/25. Resident 299 stated the PICC line was placed in the facility.
Review of Resident 299's Order Summary Report dated 5/13/25, showed a physician's order dated 5/6/25,
to change the dressing on the central line once a week and as needed. However, further review of the
physician's order failed to show documented evidence of a physician's order to measure the length of the
PICC line external catheter and the arm circumference.
Review of Resident 299's care plan for PICC use dated 5/6/25, failed to include the measurements of the
length of the external catheter and the arm circumference of Resident 299.
Review of Resident 299's TAR for May 2025 showed on 5/11/25, the PICC line dressing was changed by
the licensed nurse. However, there was no documented evidence the licensed nurse obtained the
measurements of the length of the external catheter and arm circumference of Resident 299 during the
dressing change.
On 5/14/25 at 0821 hours, an interview and concurrent medical record review for Resident 299 was
conducted with LVN 1. LVN 1 verified Resident 299 had a PICC line on the left upper arm. LVN 1 stated
they would make sure the PICC line was clean and there were no signs and symptoms of infection. LVN 1
stated the RNs were responsible for the care and maintenance of the residents' central lines.
On 5/14/25 at 0905 hours, an interview and concurrent medical record review for Resident 299 was
conducted with RN 1. RN 1 stated the RNs were responsible for the care and maintenance of the central
lines including the assessment and administration of the IV medications. RN 1 stated the assessment
included the monitoring of the PICC line insertion site for any signs and symptoms of infection and
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 7 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
documentation on the IV MAR and TAR. RN 1 stated Resident 299's PICC line on the left upper arm was
placed in the facility by the contracted provider for IV antibiotic medication administration. RN 1 stated the
dressing change for Resident 299's PICC line was done every seven days. RN 1 was asked if the
assessment of the PICC line placement would include the measurements of the length of the external
catheter of the PICC line and arm circumference, RN 1 stated yes, during dressing change. RN 1 verified
and acknowledged the PICC line assessment did not include the measurements of the length of the
external catheter and the arm circumference. Also, RN 1 verified there was no physician's order obtained
for Resident 299's PICC line for the measurements of the length of the external catheter and arm
circumference and not included in the care plan interventions.
On 5/14/25 at 0936 hours, an interview and concurrent medical record review for Resident 299 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:
555295
If continuation sheet
Page 8 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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** 2. Review of
the facility's P&P titled CPAP/BiPAP Support revised 3/2015 showed to review the physician's order to
determine the oxygen concentration and flow, and the PEEP pressure for the machine. Review and follow
manufacturer's instruction for CPAP machine setup and oxygen delivery. Under the general guidelines for
cleaning showed the following:
Residents Affected - Few
- Machine cleaning: to wipe the machine with soapy water and rinse at least once a week and as needed.
- Humidifier (if used): use clean, distilled water only in the humidifier chamber; to clean the humidifier
weekly and air dry; and to disinfect using vinegar-water solution (1:3) in the clean humidifier. To soak for 30
minutes and rinse thoroughly.
- Filter cleaning: to rinse the washable filter under running water once a week to remove dust and debris.
- Mask and nasal pillows: to wipe with isopropyl alcohol daily after use.
- Tubings and headgear (strap): to wash with soapy water, rinse, and air dry weekly.
Review of the ResMed AirSence 10 (CPAP machine) user guide (undated) showed under the caring for the
device section, to regularly clean the tubing assembly, water tub, and mask to prevent the growth of the
germs that can adversely affect the health; and clean the device weekly as directed.
On 5/12/25 at 1022 hours, an observation and concurrent interview was conducted with Resident 297.
Resident 297 was in bed awake and the CPAP machine was placed on top of the bedside drawer. Resident
297 verified the CPAP machine was her machine, and stated she cleaned and maintained the machine with
the assistance of her family member. Resident 297 stated the facility staff did not do anything about the
CPAP machine. Resident 297 stated she placed it on herself at night and took it off when she woke up.
Medical record review for Resident 297 was initiated on 5/13/25. Resident 297 was admitted to the facility
on [DATE].
Review of Resident 297's medical record failed to show documented evidence a physician's order was
obtained for the use of CPAP machine, a care plan was formulated, care and maintenance and monitoring
of the device was completed.
On 5/13/25 at 1412 hours, an interview was conducted with CNA 1. CNA 1 stated she was aware of
Resident 297's CPAP machine at the bedside and had not seen Resident 297 using the device. CNA 1
stated she was responsible for making sure the CPAP machine was in a safe place, and the mask and
tubing were placed in a clear plastic bag.
On 5/13/25 at 1226 hours, an interview and concurrent medical record review for Resident 297 was
conducted with LVN 2. LVN 2 stated the night nurses were responsible for applying the CPAP machine and
taking it off from the residents. LVN 2 verified Resident 297's used the CPAP machine. LVN 2 stated the
licensed nurses documented the care and maintenance of the CPAP machine in the TAR. LVN 2
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 9 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
reviewed Resident 297's medical record and verified there was no documented evidence of the CPAP
machine care and maintenance. LVN 2 verified and acknowledged Resident 297's CPAP machine did not
have a physician's order, care plan, and no care or maintenance of the device.
On 5/15/25 at 1040 hours, an interview and concurrent medical record review for Resident 297 was
conducted with the DON. The DON stated the residents who have a CPAP machine, the licensed nurses
would obtain a physician's order for the use, care and maintenance per the manufacturer's guidelines of the
device, formulate a care plan, and monitor the residents for the use of the device. The DON was informed
and verified the above findings.
Based on observation, interview, medical record review, and facility P&P review, the facility failed to provide
the necessary respiratory care and services for three of 13 final sampled residents (Residents 19, 40, and
397) and one nonsampled resident (Resident 297) reviewed for oxygen therapy.
* The facility failed to ensure Resident 19 was properly receiving oxygen when the nasal cannula delivering
oxygen was found on the floor.
* The facility failed to ensure Resident 40 was administered oxygen as ordered by the physician.
* The facility failed to ensure Resident 297's CPAP machine was cleaned as per the manufacturer's
guidelines and failed to obtain a physician's order, formulate a care plan, and monitor for the use of the
CPAP machine. These failures had the risk for equipment contamination and respiratory complications,
which might adversely affect the health and well-being of Resident 297.
* The facility failed to follow the physician's order for Resident 397's oxygen therapy. In addition, the facility
failed to ensure Resident 397's oxygen signage was posted on the door.
These failures had the potential for the residents to not receive the appropriate care and may negatively
impact on the residents' medical conditions.
Findings:
1. Review of the facility's P&P titled Oxygen Administration revised date 10/2010 showed to verify if there is
a physician's order for this procedure and to review the physician's orders or facility protocol for oxygen
administration. Place an Oxygen in Use sign on the outside of the room entrance door.
Medical record review for Resident 397 was initiated on 5/12/25. Resident 397 was admitted to the facility
on [DATE].
Review of Resident 397's H&P examination dated 5/7/25, showed Resident 397 had the capacity to make
decisions.
Review of Resident 397's Care Plan Report dated 5/12/25, showed a care plan focus addressing the
resident's pneumonia. The interventions included to administer the oxygen as needed as ordered for SOB
and to keep the oxygen saturation level greater than 92%.
Review of Resident 397's Order Summary Report dated 5/14/25, showed a physician's order dated
5/12/25, to administer oxygen at two LPM via nasal cannula every shift to keep the oxygen saturation
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 10 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
level greater than 92%.
Level of Harm - Minimal harm
or potential for actual harm
On 5/13/25 at 0901 hours, during an observation, Resident 397 was lying in bed with the oxygen on via
nasal cannula which was attached to the oxygen concentrator machine and set at two LPM. In addition,
during the observation, the oxygen tubing was labeled and dated; however, there was no oxygen signage
posted on the door.
Residents Affected - Few
On 5/13/25 at 1007 hours, an observation and concurrent interview was conducted with LVN 2. LVN 2
verified there was no oxygen signage on the resident's door and stated there should have been a signage
for No Smoking, Oxygen in Use for safety and awareness.
On 5/14/25 at 0829 hours, during an observation, Resident 397 was lying in bed with the oxygen on via
nasal cannula which was attached to the oxygen concentrator machine and set at one LPM.
On 5/14/25 at 0834 hours, an interview and concurrent medical record review was conducted with RN 3.
RN 3 verified the above findings and stated she would adjust the oxygen setting to two LPM and the
physician's order for the oxygen administration for Resident 397 should have been followed.
3. Medical record review for Resident 19 was initiated on 5/12/25. Resident 19 was readmitted to the facility
on [DATE].
Review of Resident 19's MDS assessment dated [DATE], showed Resident 19's BIMS score was zero,
indicating severe cognitive impairment.
Review of Resident 19's Order Summary Report showed the physician's order dated 2/27/25, to administer
oxygen at two LPM via nasal cannula to keep oxygen saturation level above 92% as needed for hypoxemia
(a condition characterized by abnormally low levels of oxygen in the blood).
On 5/13/25 at 0831 hours, an observation of Resident 19 and concurrent interview was conducted with LVN
5. Resident 19 was lying in bed and asleep. Resident 19's oxygen concentrator was turned on and set at
two LPM. However, the nasal cannula tubing was on the floor and not on Resident 19. LVN 4 verified the
findings, removed the oxygen tubing from the floor, and replaced it with a new nasal cannula. LVN 4 stated
the nasal cannula tubing was not supposed to be on the floor.
On 5/15/25 at 1505 hours, an interview was conducted with the DON. The DON was asked about the
facility's policy of oxygen tubing care and storage. The DON stated the oxygen tubing should not be on the
floor and must be kept in the bag if it was not in use or administered on the resident when in use. The DON
and Administrator were informed and acknowledged the above findings.
4. Review of the facility's P&P titled Oxygen Administration dated 10/2010 showed the following:
- Verify and review the physician's orders for oxygen administration.
- After completing the oxygen setup or adjustment, the rate of oxygen flow, route, and rationale should be
recorded in the medical record.
On 5/12/25 at 1007 hours, during the initial tour of the facility, Resident 40 was in bed receiving four LPM of
oxygen via nasal cannula.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 11 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
Level of Harm - Minimal harm
or potential for actual harm
On 5/15/25 at 1104 hours, during an observation, Resident 40 was sitting up in a chair receiving four LPM
of oxygen via nasal cannula.
Medical record review for Resident 40 was initiated on 5/15/25. Resident 40 was admitted to the facility on
[DATE]/25.
Residents Affected - Few
Review of Resident 40's Order Summary Report dated 5/15/25, showed a physician's order dated 4/10/25,
to administer oxygen at two LPM per nasal cannula every shift.
On 5/15/25 at 1111 hours, an interview and concurrent medical record review for Resident 40 was
conducted with LVN 2. LVN 2 verified Resident 40 was receiving four liters of oxygen. LVN 2 reviewed
Resident 40's orders and verified the physician's orders showed an order for the oxygen to be administered
at two LPM per nasal cannula. LVN 2 verified there was no order allowing the licensed staff to adjust the
oxygen settings. LVN 2 also verified the licensed staff was incorrectly selecting yes when the system
prompted them to verify Resident 40 was receiving oxygen at two LPM each shift.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 12 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 - Some
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** 5. On 5/12/25
at 1036 hours, during the initial tour of the facility, Resident 15 was asleep in bed with the bilateral half side
rails elevated at the head of the bed.
On 5/13/25 at 0923 hours, Resident 15 was observed lying in bed with the bilateral half side rails elevated.
Medical record review for Resident 15 was initiated on 5/12/25. Resident 15 was admitted to the facility on
[DATE].
Review of Resident 15's Order Summary Report dated 5/13/25, failed to show a physician's order for the
use of bilateral half side rails in bed.
Review of Resident 15's H&P examination dated 4/11/24, showed Resident 15 had a diagnosis of failure to
thrive, T12 compression fracture (a break in the twelfth thoracic vertebra (T12) located in the mid-back),
and osteoporosis (a disease that weakens bones, making them more likely to break).
Review of Resident 15's Annual MDS assessment dated [DATE], showed a BIMS score of 9 (scores of 8 to
12 suggest moderate cognitive impairment).
On 5/14/25 at 1319 hours, an interview and concurrent record review was conducted with RN 3. RN 3
verified the above findings and stated a physician's order should be in place for the used of bilateral half
side rails.
On 5/15/25 at 0805 hours, an interview and concurrent record review was conducted with RN 1. RN 1
acknowledged the above findings and stated there should be a physician's order, informed consent,
entrapment assessment, and bed rail assessment prior to the used of side rails to ensure residents' safety,
to prevent injuries and the risk of entrapment.
6. On 5/13/25 at 0926 hours, during an observation, Resident 34 was asleep in bed with the bilateral half
side rails elevated at the head of the bed.
On 5/14/25 at 1359 hours, Resident 34 was observed lying in bed with the bilateral half side rails elevated.
Medical record review for Resident 34 was initiated on 5/12/25. Resident 34 was admitted to the facility on
[DATE].
Review of Resident 34's Order Summary Report dated 5/13/25, failed to show a physician's order for the
use of bilateral half side rails in bed.
Review of Resident 34's H&P examination dated 4/10/25, showed Resident 34 was a high risk for falls and
had no capacity to exercise rights and sign necessary documents; therefore, the family would be informed
of medical condition and/or plan of treatment.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 13 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 - Some
Review of Resident 34's Quarterly MDS assessment dated [DATE], showed Resident 34 had severe
cognitive impairment. Section GG of the assessment showed Resident 34 had impairment to both upper
and lower extremities.
On 5/14/25 at 1333 hours, an interview and concurrent record review was conducted with RN 3. RN 3
verified the above findings and stated a physician's order should be in place for the use of bilateral half side
rails.
On 5/15/25 at 0805 hours, an interview and concurrent record review was conducted with RN 1. RN 1
acknowledged the above findings and stated there should be a physician's order, informed consent,
entrapment assessment, and bed rail assessment prior to the used of side rails to ensure the residents'
safety and to prevent injuries and the risk of entrapment.
7. On 5/13/25 at 0942 hours, during an observation, Resident 40 was awake in bed with the bilateral half
side rails elevated at the head of the bed.
Medical record review for Resident 40 was initiated on 5/13/25. Resident 40 was admitted to the facility on
[DATE].
Review of Resident 40's medical records failed to show the informed consent for the used of bilateral upper
side rails.
Review of Resident 40's H&P examination dated 4/11/25, showed Resident 40 had fluctuating capacity to
make decisions.
Review of Resident 40's admission MDS dated [DATE], showed a BIMS score of 10 (scores of 8 to 12
suggest moderate cognitive impairment).
Review of Resident 40's Order Summary Report dated 5/13/25, failed to show a physician's order for the
use of bilateral half side rails in bed.
On 5/14/25 at 1554 hours, an interview and concurrent record review was conducted with LVN 1. LVN 1
verified the above findings and stated there should be a physician's order prior to the used of bilateral half
side rails.
On 5/15/25 at 0805 hours, an interview and concurrent record review was conducted with RN 1. RN 1
acknowledged the above findings and stated there should be a physician's order, informed consent,
entrapment assessment, and bed rail assessment prior to the used of side rails to ensure residents' safety
and to prevent injuries and the risk of entrapment.
8. On 5/14/25 at 1127 hours, during a wound care observation, Resident 397 was awake in bed with the
bilateral half side rails elevated at the head of the bed.
Medical record review for Resident 397 was initiated on 5/12/25. Resident 397 was admitted to the facility
on [DATE].
Review of Resident 397's H&P examination dated 5/7/25, showed Resident 397 had the capacity to make
decisions.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 14 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
Review of Resident 397's admission MDS dated [DATE], showed a BIMS score of 15 (score of 13-15
suggests intact cognition).
Review of Resident 397's Order Summary Report dated 5/13/25, failed to show a physician's order for the
use of bilateral half side rails in bed.
Residents Affected - Some
Review of Resident 397's medical record failed to show the informed consent for the used of bilateral upper
side rails.
On 5/14/25 at 1347 hours, an interview and concurrent record review was conducted with RN 3. RN 3
verified the above findings and stated a physician's order should be in place for the use of bilateral half side
rails.
On 5/15/25 at 0805 hours, an interview and concurrent record review was conducted with RN 1. RN 1
acknowledged the above findings and stated there should be a physician's order, informed consent,
entrapment assessment, bed rail assessment, and care plan prior to the used of side rails to ensure
residents' safety, to prevent injuries and the risk of entrapment.
Based on observation, interview, medical record review, and facility P&P review, the facility failed to ensure
nine of nine final sampled residents (Residents 1, 2, 12, 15, 18, 19, 34, 40, and 397) and one nonsampled
resident (Resident 16) reviewed for the side rail use remained free from the accident hazards associated
with the use of the elevated side rails.
* The facility failed to obtain a physician's order and informed consent for the use of the bilateral upper side
rails for Residents 1, 2, 16, 19, 40, and 397. In addition, the facility failed to ensure the side rails
assessment was completed accurately for Resident 1.
* The facility failed to ensure the IDT meeting and determination for side rails was complete. Additionally,
the facility failed to have the physician's order for side rails, side rail consent, and evaluation for Residents
12 and 18.
* The facility failed to obtain a physician's order for the use of the bilateral upper side rails for Residents 15
and 34.
These failures had the potential to put the residents at risk for entrapment and serious injuries.
Findings:
The FDA issued a Safety Alert titled Entrapment Hazards with Hospital Bed Side Rails (1995), which
showed the residents most at risk for entrapment are those who are frail or elderly or those who have
conditions such as agitation, delirium, confusion, pain, uncontrolled body movement, hypoxia, fecal
impaction, acute urinary retention, etc., that may cause them to move about the bed or try to exit from the
bed. Entrapment may occur when a resident is caught between the mattress and bed rail or in the bed rail
itself. Inappropriate positioning or other care related activities could contribute to the risk of entrapment.
Review of the facility's P&P titled Bed Safety and Bed Rails revised on 8/2022 showed the following:
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 15 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 - Some
- The use of bed rails or side rails (including temporarily raising the side rails for episodic use during care) is
prohibited unless the criteria for use of bed rails have been met, including attempts to use alternatives,
interdisciplinary evaluation, resident assessment, and informed consent;
- If attempted alternatives do not adequately meet the resident's needs, the resident may be evaluated for
the use of bed rails. This interdisciplinary evaluation includes an evaluation of the alternatives to bed rails
which were attempted and how these alternatives failed to meet the resident's needs, resident's risk
associated with the use of bed rails, input from the resident and/or representative and consultation with the
attending physician; and
- Before using bed rails for any reason, the staff shall inform the resident or representative about the
benefits and potential hazards associated with bed rails and obtain informed consent.
1. On 5/12/25 at 0847 hours, during the initial tour, Resident 1 was observed lying in bed awake, was
oriented to name and verbally responsive. Resident 1's bed had elevated bilateral side rails. Resident 1
stated she did not use her side rails.
On 5/12/25 at 0856 hours, an observation and concurrent interview was conducted with CNA 2. Resident 1
was lying in bed with elevated bilateral upper side rails. CNA 2 stated Resident 1 used the bilateral upper
side rails for repositioning while in bed. CNA 2 verified the above findings.
Medical record review for Resident 1 was initiated on 5/14/25. Resident 1 was admitted to the facility on
[DATE].
Review of Resident 1's H&P examination dated 4/15/25, showed Resident 1 had no capacity to understand
and make decisions.
Review of Resident 1's MDS assessment dated [DATE], showed Resident 1's cognitive skills for daily
decision-making score was 3, indicating severely impaired.
Review of Resident 1's Order Summary Report for 4/2025 failed to show for a physician's order for the
bilateral upper side rails.
Further review of Resident 1's medical records failed to show for an informed consent for use of bilateral
upper side rails.
On 5/14/25 at 0909 hours, an interview was conducted with LVN 3. LVN 3 stated Resident 1 currently uses
the bilateral upper side rails for turning in bed. LVN 3 was asked about the process prior to applying side
rails, the LVN stated there must be a side rail assessment, order, consent and care plan. Furthermore, LVN
3 was asked who completed the entrapment assessment. LVN 3 stated she had not heard or seen an
entrapment assessment.
On 5/14/25 at 0939 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 verified Resident 1's medical record failed to show the side rails evaluation, entrapment assessments,
order, and informed consent.
2. On 5/12/25 at 0902 hours, during the initial tour, Resident 2 was lying in bed asleep. Resident 2's bed
had the elevated bilateral side rails.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 16 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 - Some
On 5/12/25 at 0905 hours, an observation and concurrent interview was conducted with CNA 2. Resident 1
was lying in bed with bilateral upper side rails elevated. CNA 2 stated Resident 2 used the bilateral upper
side rails for repositioning while in bed. CNA 2 verified the above findings.
On 5/13/25 at 0837 hours, an observation and concurrent interview was conducted with LVN 4. Resident 2
was sitting up in bed and eating her breakfast. Resident 2's bed had the elevated bilateral upper side rails.
LVN 4 verified the above findings.
Medical record review for Resident 2 was initiated on 5/14/25. Resident 2 was readmitted to the facility on
[DATE].
Review of Resident 2's MDS assessment dated [DATE], showed Resident 2's cognitive skills for daily
decision-making score was 3, indicating severely impaired.
Review of Resident 2's Order Summary Report dated 5/14/25, failed to show the physician's order for the
bilateral upper side rails.
Reviewed Resident 2's Side Rail Evaluation Quarterly dated 3/28/25, showed the Side Rails/Assist bar
were not indicated at this time.
Review of Resident 2's medical record failed to show the consent was obtained for the use of bilateral
upper side rails.
On 5/14/25 at 1028 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 verified Resident 2's medical record failed to show there was a physician's order and informed
consent from the resident's responsible party for the use of the side rails.
3. Medical record review for Resident 16 was initiated on 5/14/25. Resident 16 was readmitted to the facility
on [DATE].
Review of Resident 16's H&P examination dated 9/22/23, showed Resident 16 had the capacity to
understand and make decisions.
Review of Resident 16's MDS assessment dated [DATE], showed Resident 16's BIMS score was 15,
indicating cognitively intact.
On 5/14/25 at 0900 hours, an observation and concurrent inteview was conducted with Resident 16.
Resident 16 was in bed, awake, alert, and verbally responsive. Resident 16's bed had the elevated bilateral
upper side rails. Resident 16 stated he used the side rails for bed mobility and during transfers.
Review of Resident 16's Order Summary Report dated 5/14/25, failed to show there was a physician's
order for the use of the bilateral upper side rails.
Further review of Resident 16's medical record failed to show an informed for the use of bilateral upper side
rails.
On 5/14/25 at 0915 hours, an interview and concurrent medical record review was conducted with LVN 3.
LVN 3 reviewed the resident's medical record and verified the findings. LVN 3 stated when the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 17 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
resident had the side rails, they should have a physician's order and an informed consent.
Level of Harm - Minimal harm
or potential for actual harm
4. On 5/12/25 at 0858 hours, an initial tour observation and concurrent interview was conducted with CNA
2. Resident 19 was lying in bed, awake, alert, and eating her breakfast. Resident 19's bed had the elevated
bilateral upper side rails. CNA 2 verified the above findings. CNA 2 stated Resident 19 used the bilateral
upper side rails to reposition in bed.
Residents Affected - Some
Medical record review for Resident 19 was initiated on 5/14/25. Resident 19 was readmitted to the facility
on [DATE].
Review of Resident 19's MDS assessment dated [DATE], showed Resident 19's BIMS score was zero,
indicating severe cognitive impairment
Reviewed Resident 19's Side Rail Evaluation Quarterly dated 4/23/25, showed the Side Rails/Assist bar
were not indicated at this time.
Review of Resident 19's Order Summary Report dated 4/2025 failed to show the physician's order to apply
the bilateral upper side rails.
Review of Resident 19's medical record failed to show an informed consent for the use of bilateral upper
side rails.
On 5/14/25 at 0939 hours, an interview was conducted with RN 1. RN 1 was asked about the facility's
process prior to applying side rails. RN 1 stated the residents must be assessed for the side rails' indication,
and they need to obtain physician's order and informed consent from the resident or responsible party. RN
1 stated an entrapment assessment must be included prior to applying the side rails. RN 1 stated the
Maintenance Supervisor was responsible for the bed inspection, and the Safety Alarms/Bedrail
use/Entrapment Risk Evaluations were completed by the admission nurse and IDT. RN 1 stated the side
rails and devices used without appropriate assessments, the order and consent would be considered
physical restraint and could cause injury to the residents.
On 5/14/25 at 1010 hours, a follow-up interview and concurrent medical record review was conducted with
RN 1. RN 1 verified the above findings.
On 5/15/25 at 1505 hours, an interview was conducted with the DON and Administrator. The DON was
asked for the facility's process prior to side rail use. The DON stated she was responsible for the monthly
check of the side rail's assessments and consents completion and accuracy. The DON stated each time a
resident needed the side rails, the licensed nurse must assess for appropriateness, obtain the physician's
order and consent from the resident or responsible party, develop a care plan, complete the entrapment
assessment, and apply the side rails. The DON stated if the side rails were applied to the resident's bed
and used by the resident; however, there were no assessments, physician's order, consent, and care plan,
then the side rails should not be applied and would be considered a restraint. The DON and Administrator
were informed and acknowledged the above findings.
9. On 5/12/25 at 1054 hours and on 5/14/25 at 0835 hours, Resident 12 was observed in bed with elevated
bilateral upper side rails.
Medical record review for Resident 12 was initiated on 5/14/25. Resident 12 was admitted to the facility on
[DATE].
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 18 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 - Some
Review of Resident 12's Safety Alarms/Bedrail Use/And Entrapment Risk Evaluation dated 9/17/24,
showed the IDT Determination for bedrails was left blank. Further review of Resident 12's Entrapment Risk
Evaluation showed only one signature from the nursing department for the IDT meeting, resulting in an
incomplete IDT meeting
Review of Resident 12's Informed Consent for Bedrail Use dated 9/19/24, showed no indications were
specified for the use of side rails.
Review of Resident 12's medical record did not show the Side Rail Evaluation was completed in
conjunction with the 9/19/24 consent.
Review of Resident 12's Side Rail Evaluation - Quarterly/Annual dated 3/13/25, showed the side rails/assist
bar were not indicated at this time; however the facility entered a new Side Rail Evaluation on 5/14/25,
which showed the side rails/assist bar were indicated and served as an enabler to promote independence.
Review of Resident 12's Order Summary Report dated 5/14/25, did not show a physician's order for the use
of the side rails. Further review of the Order Summary Report showed a new order dated 5/14/25, for side
rails, quarter. There was no indication listed for the use of side rails.
On 5/14/25 at 1401 hours, an interview and concurrent medical record review for Resident 12 was
conducted with LVN 3. LVN 3 verified the IDT determination for bedrails section was blank. LVN 3 verified
the IDT meeting was incomplete because the IDT meeting should consist of members of the care team like
the physician and social worker. LVN 3 was unable to locate the physician's order for side rails prior to
5/14/25. LVN 3 verified the physician's order dated 5/14/25, was incomplete because the orders for the side
rails need to have an indication. LVN 3 verified the consent dated 9/19/24, was incomplete because there
were no indications for side rails listed and stated indications were necessary because the side rails were
considered an assistive device, and could be considered a restraint. LVN 3 was unable to locate an
assessment associated with the consent dated 9/19/24. LVN 3 verified the side rails should not have been
in use for Resident 12 because the evaluation dated 3/13/25, showed side rails were not indicated.
10. On 5/12/25 at 1045 hours and on 5/14/25 at 0835 hours, Resident 18 was observed in bed with
elevated bilateral upper side rails.
Medical record review for Resident 18 was initiated on 5/14/25. Resident 18 was admitted to the facility on
[DATE].
Review of Resident 18's Safety Alarms/Bedrail Use/And Entrapment Risk Evaluation dated 2/5/25, showed
the sections for the Bedrail Evaluation Summary and IDT Determination for bedrails were left blank. Further
review of Resident 18's Entrapment Risk Evaluation showed only one signature from the nursing
department for the IDT meeting, resulting in an incomplete IDT meeting
Review of Resident 18's Informed Consent for Bedrail Use dated 3/1/25, showed no indications were
specified for the use of side rails.
Review of Resident 18's Side Rail Evaluation dated 3/27/25, showed the side rails/assist bar were not
indicated at this time.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 19 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
Review of Resident 18's Order Summary Report dated 5/14/25, did not show an order for side rails.
Level of Harm - Minimal harm
or potential for actual harm
On 5/14/25 at 1401 hours, an interview and concurrent medical record review for Resident 18 was
conducted with LVN 3. LVN 3 verified the bedrail evaluation summary and the IDT Determination were
incomplete because there was no documentation. LVN 3 verified the IDT meeting was incomplete because
the IDT meeting should consist of members of the care team like the physician and the social worker. LVN 3
was unable to locate a physician's order for side rails prior to 5/14/25. LVN 3 verified the consent dated
3/1/25, was incomplete because there were no indications for the side rails listed and stated the indications
were necessary because the side rails were considered an assistive device and could be considered as a
restraint. LVN 3 verified the side rails should not have been in use for Resident 18 because the evaluation
dated 3/27/25, showed the side rails were not indicated.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 20 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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** 2. Review of
the facility's P&P titled Medication Administration Subcutaneous dated 2007 showed the licensed nurses to
administer medications via the subcutaneous route in a safe, accurate and effective manner. The
procedures included the following:
- To check the last injection sites and select a new appropriate site for injection.
- To document the injection on the MAR along with the site.
Medical record review for Resident 597 was initiated on 5/13/25. Resident 597 was admitted to the facility
on [DATE].
On 5/14/25 at 1410 hours, an observation and concurrent interview was conducted with Resident 597.
Resident 597 was in his wheelchair awake with bluish to greenish discoloration on the posterior right upper
arm. Resident 597 stated the nurse gave his injection medication for blood clot on the back of his arm.
Review of Resident 597's Order Summary Report dated 5/14/25, showed a physician's order dated
4/29/25, to administer enoxaparin sodium injection 40 mg subcutaneously one time a day for DVT
prophylaxis for 21 days.
Review of Resident 597's Location of Administration Report for April and May 2025 for Resident 597's
enoxaparin injection showed the injection sites were not rotated on the following dates and times:
- on 4/26/25 at 0849 hours, the enoxaparin medication was administered to the left rear of the upper arm.
- on 4/27/25 at 0943 hours, the enoxaparin medication was administered to the left rear of the upper arm.
- on 4/29/25 at 0844 hours, the enoxaparin medication was administered to the left rear of the upper arm.
- on 4/30/25 at 0828 hours, the enoxaparin medication was administered to the left rear of the upper arm.
- on 5/1/25 at 0925 hours, the enoxaparin medication was administered to the left rear of the upper arm.
- on 5/2/25 at 0842 hours, the enoxaparin medication was administered to the left rear of the upper arm.
- on 5/11/25 at 1005 hours, the enoxaparin medication was administered to the right rear of the upper arm.
- on 5/11/25 at 1010 hours, the enoxaparin medication was administered to the right rear of the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 21 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
upper arm.
Level of Harm - Minimal harm
or potential for actual harm
- on 5/12/25 at 1042 hours, the enoxaparin medication was administered to the right rear of the upper arm.
Residents Affected - Few
Further review of Resident 597's medical record failed to show documented evidence Resident 597's skin
discoloration on the right upper arm was assessed, monitored, and the physician and family representative
were notified.
On 5/14/25 at 1435 hours, an interview and concurrent medical record review for Resident 597 was
conducted with LVN 1. LVN 1 verified Resident 597 was on anticoagulant medication for DVT prophylaxis
and monitored for any signs and symptoms for bleeding. LVN 1 was asked if she administered the
anticoagulant medication injection to Resident 597's dose for the day. LVN 1 verified and stated she
administered the anticoagulant medication injection to Resident 597's left upper arm. LVN 1 was asked if
she observed any skin discoloration to Resident 597's right upper arm. LVN 1 denied observation of any
skin discoloration of Resident 597. LVN 1 was asked at Resident 597 bedside and assessed the skin
discoloration of the resident. LVN 1 verified the skin discoloration on the right upper arm of Resident 597.
On 5/15/25 at 0908 hours, an interview and concurrent medical record review for Resident 597 was
conducted with RN 1. RN 1 was asked at Resident 597's bedside and verified the skin discoloration on the
resident's right upper arm. RN 1 stated she was not aware and did not receive any report about the skin
discoloration of Resident 597. RN 1 verified Resident 597 was on anticoagulant medication which was
administered via injection subcutaneously. RN 1 was asked how the licensed nurse would know where the
last injection sites of the anticoagulant medication was administered. RN 1 stated the licensed nurse
documented the injection sites in the MAR under the Location of Administration Report included the date
and time of administration of the medication. RN 1 was asked to review the MAR under the Location of
Administration Report for the administration of enoxaparin. RN 1 verified and acknowledged the injection
sites for enoxaparin injection medication were not rotated on several days when the anticoagulant
medication was administered. RN 1 stated the injection sites for the anticoagulant medication should have
been rotated to different sites to prevent any adverse effects.
On 5/15/25 at 1105 hours, an interview and concurrent medical record review for Resident 597 was
conducted with the DON. The DON stated she expected the licensed nurses would follow the facility's P&P
on administering medications. The DON was informed of the findings and verified the above findings.
Based on observation, interview, medical record review, facility document review, and facility P&P, the
facility failed to provide pharmaceutical services to meet the resident's needs for one of 13 final sampled
residents (Resident 597).
* The facility failed to ensure Resident 597's oxycodone HCl IR (narcotic) was accurately reconciled.
Resident 597's oxycodone HCl was documented as administered on the Controlled Drug Record but not on
the electronic MAR. This failure had the potential for diversion of controlled medications.
* The facility failed to ensure Resident 597's enoxaparin (anticoagulant medication) injection sites were
rotated. This failure had the potential for poor health outcome for Resident 597.
Findings:
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 22 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
1. Review of the facility's P&P titled Controlled Substances dated 2007 showed to administer the controlled
medication and document the dose administration on the MAR.
On 5/12/25 at 1109 hours, a concurrent observation of Station 1's Medication Cart, interview, medical
record review for Resident 597 and facility document review was conducted with LVN 1. Review of Resident
597's Controlled Drug Record - Individual Patient's Narcotic Record showed one tablet of oxycodone HCl
was removed from the bubble pack on 5/3/25 at 2200 hours. Resident 597's oxycodone HCl bubble pack
showed eight tablets remaining, which matched the number of oxycodone HCl tablets in Resident 597's
Controlled Drug Record.
Review of Resident 597's MAR failed to show the oxycodone HCl medication was administered to the
resident on 5/3/25 at 2200 hours. LVN 1 acknowledged and verified the oxycodone HCl medication was
removed from the bubble pack on 5/3/25, and documented in Resident 597's Controlled Drug Record but
not in the MAR. LVN 1 stated the medication should have been documented in the MAR right after it was
administered.
Medical record review for Resident 597 was initiated on 5/12/25. Resident 597 was admitted to the facility
on [DATE].
Review of Resident 597's H&P examination dated 4/26/25, showed Resident 597 had no capacity to
exercise rights and sign necessary documents.
Review of Resident 597's Order Summary Report dated 4/30/25, showed a physician's order dated
4/23/25, to administer Oxycodone HCl one tablet by mouth every six hours as needed for moderate pain.
On 5/14/25 at 1043 hours, a telephone interview was conducted with RN 1. RN 1 verified she worked in the
facility on 5/3/25, during the evening shift. RN 1 stated she administered Resident 597's medications during
her shift. RN 1 stated Resident 597 complained of pain, so she gave the oxycodone HCl medication to
Resident 597 after popping it out of the bubble pack. RN 1 stated she was not sure what happened and
was sure she signed it as administered on the MAR. When asked about the process of administering the
controlled medications, RN 1 stated, I signed Resident 597's Controlled Drug Record right after I removed
the oxycodone HCl medication and signed the MAR after I administered the medication. RN 1 further
stated, I should have double checked if I signed the MAR.
On 5/14/25 at 1026 hours, a concurrent medical record review for Resident 597, facility document review,
and interview was conducted with the DON. The DON verified the findings.
On 5/15/25 at 1445 hours, an interview was conducted with the Administrator and DON. The Administrator
and DON were informed and verified the above findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 23 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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, and medical record review, the facility failed to ensure the medication error rate was
below 5%. The facility's medication error rate was 6.45%. One of two licensed nurses (LVN 1) observed
during the medication administration was found to have made errors.
Residents Affected - Few
* LVN 1 failed to ensure metformin medication (antidiabetic) was administered to Resident 26 with meal as
per the physician's orders.
* LVN 1 failed to ensure Resident 697 received calcium citrate (supplement) on time following admission to
the facility.
These failures created the risk for the residents to have potential side effects or complications related to the
medications.
Findings:
1. Review of the facility's P&P titled Administering Medications dated 4/2019 showed the following:
- Medications are administered in accordance with prescriber orders, including any required time frame
- Medications are administered within one (1) hour of their prescribed time, unless otherwise specified (for
example, before and after meal orders).
On 5/13/25 at 0908 hours, a medication administration observation for Resident 26 was conducted with
LVN 1. LVN 1 prepared one tablet of metformin 1000 mg medication. LVN 1 administered the metformin
tablet medication to Resident 26 at 0922 hours. Resident 26 stated she ate breakfast at 0800 hours.
Medical record review for Resident 26 was initiated on 5/13/25. Resident 26 was admitted to the facility on
[DATE].
Review of Resident 26's Order Summary Report showed a physician's order dated 4/8/25, for metformin
HCl oral tablet 1000 mg one tablet by mouth two times a day for DM. Take with meals.
On 5/13/25 at 1408 hours, an interview and concurrent medical record review was conducted with LVN 1.
LVN 1 verified she did not administer the metformin medication to Resident 26 with her meal.
2. Review of the facility's P&P titled Administering Medications dated 4/2019 showed the following:
- Medications and related products are received from the provider pharmacy on a timely basis. The nursing
care center maintains accurate records of medication order and receipt.
- New medications, except for emergency or stat medications, are ordered as follows:
- If the first dose of medication is scheduled to be given before the next regularly scheduled pharmacy
delivery, please telephone or transmit the medication orders to the pharmacy immediately upon receipt.
Inform the pharmacy of the need for prompt delivery.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 24 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
- Timely delivery of new orders is required so that mediation administration is not delayed.
Level of Harm - Minimal harm
or potential for actual harm
On 5/13/25 at 0853 hours, a medication administration observation for Resident 697 was conducted with
LVN 1. LVN 1 was unable to administer the calcium citrate to Resident 697 as the pharmacy had not
delivered the medication since admission.
Residents Affected - Few
Medical record review for Resident 697 was initiated on 5/13/25. Resident 697 was admitted to the facility
on [DATE].
Review of Resident 697's Order Summary Report showed a physician's order dated 4/8/25, for calcium
citrate oral tablet 950 mg (200 Ca) one tablet by mouth one time a day for supplement.
On 5/13/25 at 1000 hours, an interview and concurrent medical record review was conducted with LVN 3.
LVN 3 verified Resident 697 was admitted to the facility on [DATE] at 1410 hours.
On 5/13/25 at 1402 hours, an interview and concurrent medical record review was conducted with LVN 1.
LVN 1 stated as soon as a resident was admitted , all medication orders were sent to the pharmacy, and
the medications were usually delivered within the same day. LVN 1 verified the calcium citrate medication
had not yet been delivered.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 25 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 0804
Ensure food and drink is palatable, attractive, and at a safe and appetizing temperature.
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
ensure the food items were served in appetizing temperatures:
Residents Affected - Some
* The temperature was not maintained at the acceptable range for cold beverages. This failure posed the
risk for not providing palatable and appetizing food for the residents receiving a meal tray from the kitchen.
Findings:
Review of the facility's Diet Type Report dated 5/12/25, showed 45 of 45 residents consumed the food
prepared in the kitchen.
Review of the facility's P&P titled Cold Holding and Storage revised date 12/1/22, showed cold TCS
(Time/Temperature Control for Safety) food must be held at proper temperatures to prevent harmful
bacterial growth and/ or toxin production that can occur if it remains in the temperature danger zone too
long. Cold TCS foods must be maintained at 41 degrees Fahrenheit or below during holding, display,
service, and transport.
On 5/13/25 at 1140 hours, a tray line observation and concurrent interview was conducted with the CDM.
The CDM checked and verified the following temperatures:
- cranberry juice - 42.6 degrees Fahrenheit;
- another cranberry juice - 43.8 degrees Fahrenheit;
- orange juice - 42.8 degrees Fahrenheit; and
- mixed cranberry and orange juice - 43.6 degrees Fahrenheit.
The CDM verified the temperature of the cranberry juice, orange juice, and mixed cranberry juice were not
holding the cold beverage temperature. The CDM stated the holding temperatures for the cold beverages
should be 41 degrees Fahrenheit and below. The CDM acknowledged the beverage temperatures varying
from 42.6 to 43.8 degrees Fahrenheit were above the recommended temperatures for cold food. The
pitcher of beverages was placed in bucket of ice to keep beverages cold prior to serving the residents'
lunch.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 26 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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, facility document review, 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 the sanitary condition of the hood over the stove was maintained.
* The facility failed to ensure the kitchen utensils had a smooth cleanable surface and in good condition.
* The facility failed to ensure the kitchenware and kitchen utensils were clean and free of food particles or
residue.
* The facility failed to ensure the cutting boards were kept in a sanitary condition and with cleanable
surface.
* The facility failed to ensure the heavy-duty blenders used for puree preparation were dried and clean prior
to storing.
These failures had the potential for cross contamination and foodborne illnesses to the residents
consuming the food prepared in the facility's kitchen.
Findings:
Review of the facility's Diet Type Report dated 5/12/25, showed 45 of 45 residents consumed the food
prepared in the kitchen.
1. Review of the facility's P&P titled Sanitation and Infection Prevention/ Control, Area and Equipment
Cleaning revised date 1/2025 showed the facility's Maintenance Department is scheduled to clean
equipment that requires special training and equipment, such as the ice maker, refrigeration coils and
exhaust hood.
Review of the facility's P&P titled Equipment Condition and Management dated 10/1/22, showed the
equipment must be maintained in a state of good repair and condition, in compliance with applicable local,
state, and federal, statutes, regulations, and ordinances.
According to the USDA Food Code 2022 Section 4-204.11 Ventilation Hood Systems, Drip Prevention. The
dripping of grease or condensation onto food constitutes adulteration and may involve contamination of the
food with pathogenic organisms. Equipment, utensils, linens, and single service and single use articles that
are subjected to such drippage are no longer clean.
On 5/12/25 at 0836 hours, during the initial kitchen tour, an observation and concurrent interview was
conducted with the Dietary Aide. The kitchen hood over the stove had black, dirt residue. The Dietary Aide
acknowledged the findings.
2. Review of the facility's P&P titled Sanitation and Infection Prevention/ Control, Cleaning of Food and
Nonfood Contact Surfaces revised date 1/2025 showed discard any food contact surfaces with chips, nicks
or broken pieces, such as fryer baskets or skimmers that have damaged, loose or broken
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 27 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
wires, strainers, pans, skillets, and knives, which cannot be cleaned properly. Nonfood contact surfaces of
utensils and equipment must be made of materials that are safe, corrosion resistant, nonabsorbent, smooth
and easily cleanable, and maintained in good condition.
Review of the facility's P&P titled Equipment Condition and Management dated 10/1/22, showed the
equipment and utensils must be designed and constructed to be safe and to prevent the migration of
harmful substances, colors, odor or tastes to food. Also under normal use conditions, materials that are
used in the construction of utensils and food-contact surfaces of equipment must be smooth and free of
breaks, open seams, cracks, chips, inclusions, pits, and similar imperfections. Durable, corrosion-resistant,
and non-absorbent. Finished to have a smooth, easily cleanable surface. Resistant to pitting, chipping,
scratching, scoring, distortion, and decomposition. Free of sharp internal angles, corners, and crevices.
Finished to have smooth welds and joints.
According to the USDA Food Code 2022 Section 4-502.11 Good Repair and Calibration, (A) Utensils shall
be maintained in a state of repair and condition that complies with the requirements specified under Parts
4-1 and 4-2 or shall be discarded.
According to the USDA Food Code 2022, Section 4-101.11, Multiuse, Characteristics, materials that are
used in the construction of the utensils and food contact surfaces of equipment may not allow the migration
of deleterious substances or impart colors, odors, or tastes to food and under normal use conditions shall
be durable, corrosion-resistant, nonabsorbent, finished to have a smooth, easily cleanable surface, and
resistant to pitting, chipping, crazing, scratching, scoring, distortion, and decomposition.
On 5/12/25 at 0836 hours, during the initial kitchen tour, an observation and concurrent interview was
conducted with the Dietary Aide. The following was observed and verified by the Dietary Aide:
- One Ninja blender stored at a countertop shelf was old and worn out and cracked at the base of the
blender. The lid was cracked and the rubber portion worn out and discolored.
- One stainless steel serving spoon with black handle was partially melted.
- One stainless steel spatula with black handle was deformed at the edges and handle partially melted.
- One plastic black spoon was partially melted at the edges.
- Two rubber spatulas with red handle were chipped/cracked at the edges.
- One rubber spatula with brown handle was discolored, chipped/cracked at the edges.
- One stainless steel serving scoop with a black handle partially melted.
- Two stainless steel slotted serving scoops with black handles were partially melted.
- One stainless steel serving spoon with black handle was partially melted.
- One stainless steel spatula with brown handle was chipped at the edges and handle was discolored and
partially melted.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 28 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
- One stainless steel ice cream scoop old, worn out, and discolored.
Level of Harm - Minimal harm
or potential for actual harm
- One cutting dough with cream handle was discolored and partially melted.
Residents Affected - Some
3. Review of the facility's P&P titled Sanitation and Infection Prevention/ Control, Cleaning of Food and
Nonfood Contact Surfaces revised date 1/2025 showed the food contact surfaces are in good condition,
made of non-toxic materials and are easily cleanable. The food-contact surfaces of all the cooking
equipment shall be kept free of encrusted grease deposits and other accumulated soil.
Review of the facility's P&P titled Equipment Condition and Management dated 10/1/22, showed the
equipment and utensils must be designed and constructed to be safe and to prevent the migration of
harmful substances, colors, odor or tastes to food. Also under normal use conditions, the materials that are
used in the construction of the utensils and food-contact surfaces of the equipment must be durable,
corrosion-resistant, and non-absorbent.
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
the equipment shall be cleaned at a frequency necessary to preclude accumulation of soil residues.
On 5/12/25 at 0836 hours, during the initial kitchen tour, an observation and concurrent interview was
conducted with the Dietary Aide. The following was observed and verified by the Dietary Aide:
- Robot coupe blender at a countertop shelf with blade had dry, orange residue, rubber portion of the lid
was dirty and had yellow discoloration.
- Four stainless steel serving scoops with green handles were stored in the clear container for clean
spoodles and utensils were dirty with dry fuzzy film, watermarks and crusted residue.
- Two stainless steel serving scoops with blue handles were stored in the clear container for clean spoodles
and the utensils were dirty with dry watermarks and crusted residue.
- Two stainless steel serving scoops with cream handles were stored in the clear container for clean
spoodles and the utensils were dirty with dry watermarks and crusted residue.
- One stainless steel serving scoop with black handle was stored in the clear container for clean spoodles
and the utensil was dirty and had dry crusted residue.
- Two stainless steel serving spoons with black handles were stored in the clear container for clean
spoodles and the utensils were dirty, had dry watermarks and crusted residue.
- Two stainless steel serving slotted scoops with black handles were stored in the clear container for clean
spoodles and the utensils were dirty, had dry fuzzy film and crusted residue.
- One stainless steel slotted serving spoon was stored in the clear container for clean spoodles
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 29 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
and the utensil was dirty with crusted residue.
Level of Harm - Minimal harm
or potential for actual harm
- One stainless steel scoop with a blue handle used for food portioning was stored in the clear container for
clean spoodles and the utensil was dirty and had crusted residue.
Residents Affected - Some
- One stainless steel scoop with gray handle used for food portioning was stored in the clear container for
clean spoodles and the utensil was dirty and had crusted residue.
- One stainless steel serving scoop with black handle was stored in the clear container for clean spoodles
and the utensils was dirty and had dry crusted residue.
- Two stainless steel slotted serving scoops with black handles were stored in the clear container for clean
spoodles and the utensils were dirty and had dry crusted residue.
- One stainless steel serving spoon with black handle was stored in the clear container for clean spoodles
and the utensil was dirty with dry watermarks.
4. Review of the facility's P&P titled Equipment Condition and Management dated 10/1/22, showed surfaces
such as the cutting blocks and boards that are subject to scratching and scoring must be resurfaced if they
can no longer be effectively cleaned and sanitized or discarded if they are not capable of being resurfaced.
According to the USDA Food Code 2022, Section 4-501.12, Cutting Surfaces, for surfaces such as the
cutting boards and blocks that become scratched and scored may be difficult to clean and sanitize. As a
result, pathogenic microorganisms transmissible through food may build up or accumulate. These
microorganisms may be transferred to the foods that are prepared on such surfaces.
On 5/12/25 at 0836 hours, an initial tour observation and concurrent interview was conducted with the
Dietary Aide. The white, green, and red cutting boards were observed fuzzy, discolored, heavily marred and
had deep groves. The Dietary Aide verified the findings, and stated the cutting boards were ordered by the
Chef, and was unsure how often.
5. Review of the facility's P&P titled Dish Machine Usage and Testing dated 10/1/22, showed for air dry:
place the equipment or utensils onto a clean surface to air dry. Do not dry with a towel or other method.
According to the USDA Food Code 2022, 4-901.11, Equipment and Utensils, Air-Drying Required, that after
cleaning and sanitizing, the equipment, and utensils shall be air-dried or used after adequate draining
before getting in contact with food.
According to the USDA Food Code 2022, 4-903.11 Equipment, Utensils, Linens, and Single-Service and
Single-Use Articles, the cleaned equipment and utensils shall be stored in a self-draining position that
allows air drying.
On 5/12/25 at 0836 hours, an initial tour observation and concurrent interview was conducted with the
Dietary Aide. Two heavy-duty blenders stored at a countertop shelf were still wet with water dripped from
the blender lid and visible water inside. The Dietary Aide acknowledged the above findings.
The Director of Dining Services was informed and acknowledged all the above findings. The Director
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 30 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
of Dining Services stated all the utensils should have been washed properly to prevent bacteria growth and
for infection control purposes. The blenders should have been air dried to prevent mold and bacteria
growth. The cutting boards should have been replaced for infection control purposes. The hood over the
stove should be free from grease or dirt for fire hazard prevention.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 31 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 0838
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Conduct and document a facility-wide assessment to determine what resources are necessary to care for
residents competently during both day-to-day operations (including nights and weekends) and
emergencies.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and facility document review, the facility failed to ensure the Facility Assessment addressed or
included the following:
1. Active involvement of required individuals in developing the Facility Assessment;and
2. A contingency plan for staffing needs.
This failure had the potential not to meet the residents' care needs if the assessed population's needs and
resources were not comprehensively identified and addressed.
Findings:
According to the CMS QSO-24-13-NH dated 6/18/24, with an implementation date of 8/8/24, the CMS
issued revised guidance for long-term care facility assessment requirement. The Facility Assessment
should address and included the active involvement of the direct care staff in developing the Facility
Assessment. There should also be a contingency plan for staffing needs for events so as not to activate the
facility's emergency plan.
Review of the Facility's assessment dated [DATE], did not show the direct care staff members, direct care
representatives, residents, residents' representatives, and residents' family members were actively involved
in developing the Facility Assessment. Additionally, the Facility Assessment did not show resources
necessary to care for the residents including a contingency plan for the staffing needs.
On 5/15/25 at 1019 hours, an interview and concurrent facility document review of the Facility Assessment
was conducted with the Administrator. The Administrator verified the Facility Assessment was dated
3/12/25, and acknowledged she was aware of the new update of the Facility Assessment from the CMS.
The Administrator verified there were no direct care staff, direct care representatives, residents, resident
representatives, and family members actively involved in developing the Facility Assessment. The
Administrator further verified there were no contingency plan for the staffing needs. The Administrator
verified and acknowledged the Facility Assessment was not updated based on the latest update from the
CMS.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 32 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 - Potential for
minimal harm
Residents Affected - Some
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** Based on
interview, medical record review and facility P&P review, the facility failed to ensure the medical record for
one of 13 final sampled residents (Resident 298) was complete and accurate. This failure had the potential
for Resident 298's care needs not being met as the medical record was inaccurate.
Findings:
Review of the facility's P&P on Output Measuring and Recording dated October 2010 showed the following:
- Purpose: to accurately determine the amount of urine a resident excretes in a 24-hour period;
- Documentation: the amount of urine output in ml should be recorded in the resident's medical record.
Medical record review for Resident 298 was initiated on 5/15/25. Resident 298 was admitted on [DATE].
Review of Resident 298's Order Summary Report dated 5/15/25, showed the following orders:
- dated 4/29/25, for intake and output every shift;
- dated 5/11/25, for urinary catheter 18 Fr with 10 cc bulb every shift; and
- dated 5/11/25, to drain catheter every shift.
Review of Resident 298's TAR failed to show the urine output recorded on the following dates and shifts:
- 5/3/25, for both day and night shifts.
- 5/7/25, for the night shift.
- 5/8/25, for the evening shift.
- 5/9/25, for the night shift.
- 5/11/25, for the evening.
On 5/15/25 at 0940 hours, a telephone interview and concurrent medical record review was conducted with
RN 1 and the DON. RN 1 confirmed Resident 298 had an indwelling urinary catheter in place. RN 1 verified
the incomplete entries and stated the output measured should have been recorded with the actual amount
of urine. The DON verified the above findings and stated the nurses were responsible for checking the
output and documenting in the TAR.
On 5/15/25 1445 hours, an interview was conducted with the Administrator and DON. The Administrator
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 33 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
and DON verified the above findings.
Level of Harm - Potential for
minimal harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 34 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
3. Review of the facility's P&P titled Bedpan/ Urinal Offering/ Removing dated 2/2018 showed store the
bedpan or urinal as per facility policy.
Residents Affected - Few
Review of the facility's P&P titled Handwashing/ Hygiene dated 8/2019 showed the use of an alcohol-based
hand rub at least 62% alcohol or alternatively, soap (antimicrobial or non- antimicrobial) and water: after
handling contaminated equipment.
On 5/12/25 at 1242 hours, an observation in Resident 597's room and concurrent interview was conducted
with CNA 5. Resident 597's urinal containing urine was observed on top of the overbed table near
uncovered cups of water and cranberry juice. CNA 5 entered the room, put on gloves, removed the urinal,
and discarded the urine to the toilet, rinsed the urinal, and placed the urinal back to Resident 597's overbed
table near the uncovered cups of water and cranberry juice. CNA 5 used the same gloves previously used
to discarding the contents of the urinal, to move the overbed table and put on socks to Resident 597's feet.
CNA 5 acknowledged the urinal was on top of the over bed table and verified he should not have placed the
urinal back to the overbed table. CNA 5 further stated the urinal should be kept away from food or drinks.
CNA 5 acknowledged and verified he did not remove the gloves he wore when he discarded the urine from
the urinal and continued with what he was doing. CNA 5 was asked if using the same contaminated gloves
in moving the table or putting on resident's socks were acceptable, CNA 5 stated No, I should have
changed my gloves and washed my hands.
On 5/12/25 at 1246 hours, an observation and concurrent interview was conducted with the IP. The IP
observed the urinal on top of the overbed table and verified the urinal should not be on top of the overbed
table. The IP verified the above findings.
On 5/15/25 at 1100 hours, an observation and concurrent interview was conducted with the DON. The DON
verified the findings and stated the facility's policy required the urinals be placed in the designated urinal
holders at bedside and should not be placed on the over bed table or the nightstand.
On 5/15/25 at 1445 hours, an interview was conducted with the Administrator and DON. The Administrator
and DON verified all of the above findings.
Based on observation, interview, medical record review, facility document review, and facility P&P review,
the facility failed to maintain the infection control program designed to help prevent the development and
transmission of diseases and infections.
* The facility failed to ensure the staff's personal belongings were not stored with the clean linen.
* The facility failed to ensure LVN 6 performed hand hygiene when providing wound care treatment to
Resident 19.
* CNA 5 placed Resident 597's urinal near the cups of beverages and failed to perform hand hygiene after
handling a urinal.
These failures posed the risk for not identifying infections and controlling the transmission of communicable
disease to other residents throughout the facility.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 35 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
Findings:
Level of Harm - Minimal harm
or potential for actual harm
1. Review of the facility's P&P titled Laundry Infection Control revised on 11/2023 showed the following:
- Clean linen shall be handled, transported, and stored by methods that will ensure its cleanliness.
Residents Affected - Few
Review of the facility's P&P titled Laundry Supplies Storage revised on 11/2023 showed the supply area
must be neat organized and locked at all times.
On 5/14/25 at 1115 hours, during the initial tour, the black backpack and jacket were stored with the clean
linen in the clean linen room.
On 5/14/25 at 1118 hours, an observation and concurrent interview was conducted with the Laundry Aide
and the Housekeeping Supervisor. The Laundry Aide and the Housekeeping Supervisor verified the above
findings. The Laundry Aide stated the black backpack and jacket stored with the clean linen were his
personal belongings. In addition, the Laundry Aide stated his personal belongings were not supposed to be
stored with the clean linen.
On 5/15/25 at 1505 hours, an interview was conducted with the Administrator. The Administrator was asked
about the facility's policy in storing employee's belongings in the laundry clean area. The Administrator
stated the employee's personal belongings should not to be stored with the clean linens. Furthermore, the
Administrator stated the laundry's clean linen area must be always kept clean.
2. Review of the facility's P&P titled Handwashing and Hand Hygiene revised on 8/2019 showed the
following:
- All personnel staff follow the handwashing/hand hygiene procedures to help prevent the spread of
infections to other personnel, residents, and visitors;
- Wash hands with soap (antimicrobial or non-antimicrobial) and water for the following situations like when
hands are visibly soiled and after contact with a resident with infectious diarrhea including but not limited to
infections caused by norovirus (a group of viruses that causes severe vomiting and diarrhea), salmonella
(bacteria that causes diarrhea, fever and stomach pains), shigella (are bacteria (germs) that cause
diarrhea), and C. difficile (a bacterial infection that can cause diarrhea and other symptoms, including
colitis, which is inflammation of the colon);
- Use an alcohol-based hand rub containing at least 62% alcohol or alternatively soap and water for the
following situations like before and after direct contact with residents, before performing any non-surgical
invasive procedures, before handling clean or soiled dressings or gauze, after contact with resident's intact
skin and after removing gloves; and
- The use of gloves does not replace hand washing or hand hygiene. Integration of glove use along with
routine and hygiene is recognized as the best practice for preventing healthcare-associated infections.
On 5/13/25 at 0936 hours, a wound care observation for Resident 19 and a concurrent interview was
conducted with LVN 5. LVN 5 stated Resident 19 had a sacrococcyx pressure injury (localized skin
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 36 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
damage caused by prolonged or intense pressure, often over bony prominences). The following was
observed:
- LVN 5 was performed hand hygiene with an alcohol-based hand rub, then donned clean gloves and
explained the procedure to the resident;
Residents Affected - Few
- LVN 5 touched Resident 19's right thigh after picking up the trash can with the same gloves without
performing hand hygiene;
- LVN 5 removed the gloves, donned clean gloves, and removed Resident 19's dressing on the sacrococcyx
without performing hand hygiene;
- LVN 5 cleaned Resident 19's sacrococcyx pressure injury with a gauze soaked with normal saline, patted
dry with dry gauze, applied Collagen powder (a topical wound treatment, particularly for promoting healing
in stalled or chronic wounds, and can be an effective adjunctive therapy) and calcium alginate (a naturally
derived, highly absorbent wound dressing material made from seaweed to treat various wounds), and
covered with a foam dressing without changing gloves and performing hand hygiene; and
- LVN 5 removed the gloves and washed her hands after the wound care treatment.
On 5/13/25 at 0956 hours, a follow-up interview was conducted with LVN 5. When asked about performing
a hand hygiene during wound care treatment, LVN 5 stated infection control practices like handwashing and
hand hygiene must be performed to prevent the spread of infection to Resident 19 especially after touching
a dirty trash receptacle. LVN 5 verified the above findings.
Review of Resident 19's Order Summary Report showed physician's order dated 5/12/25, showed to
cleanse the sacrococcyx pressure injury with normal saline, pat dry, apply Collagen powder and Calcium
alginate then cover with a foam dressing daily and as needed for soiling for 14 days.
On 5/15/25 at 1505 hours, an interview was conducted with the DON. The DON was asked about the
facility's infection control policy, especially during wound care treatment. The DON stated the licensed nurse
or treatment nurse must remove the gloves after touching any dirty surfaces, perform handwashing, and
don new gloves to prevent the spread of infection. The DON and Administrator were informed and
acknowledged the above findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 37 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 - Some
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** Based on
observation, interview, medical record review, facility document review, and facility P&P review, the facility
failed to ensure the residents' entrapment assessments were accurately completed for nine of 13 final
sampled residents (Residents 1, 2, 12, 15, 18, 19, 34, 40, and 397) and one nonsampled resident
(Resident 16). This failure had the potential to negatively impact the residents, resulting in possible
entrapment, serious injury, and death.
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 and Bed Rails revised date 8/2022 showed the resident beds
meet the safety specifications established by the Hospital Bed Safety Workgroup. The use of bed rails is
prohibited unless the criteria for use of bed rails have been met. Consideration is given to the resident's
safety, medical conditions, comfort, and freedom of movement, as well as input from the resident and family
regarding previous sleeping habits and bed environment. Bed frames, mattresses and bed rails are
checked for compatibility and size prior to use. Bed dimensions are appropriate for the resident's size.
Maintenance staff routinely inspects all beds and related equipment to identify risks and problems including
potential entrapment risks.
Review of the facility's Bed System Measurement Device Test Results Worksheet (undated) failed to show
Zones 6 and 7 were reflected and recorded on the form and assessed for entrapment. For example:
1. On 5/12/25 at 1036 hours, during the initial tour of the facility, Resident 15 was asleep in bed with the
bilateral half side rails elevated at the head of the bed.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 38 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
On 5/13/25 at 0923 hours, Resident 15 was observed lying in bed with the bilateral half side rails elevated.
Level of Harm - Minimal harm
or potential for actual harm
Medical record review for Resident 15 was initiated on 5/12/25. Resident 15 was admitted to the facility on
[DATE].
Residents Affected - Some
Review of Resident 15's H&P examination dated 4/11/24, showed Resident 15 had a diagnosis of failure to
thrive, T12 compression fracture (a break in the twelfth thoracic vertebra (T12) located in the mid-back),
and osteoporosis (a disease that weakens bones, making them more likely to break).
Review of Resident 15's Annual MDS assessment dated [DATE], showed a BIMS score of 9 (scores of 8 to
12 suggest moderate cognitive impairment).
Review of Bed System Measurement Device Test Results Worksheet dated 5/1/25, failed to show Zones 6
and 7 were reflected and recorded on the form and assessed for the entrapment.
Cross reference to F700, example #5.
2. On 5/13/25 at 0926 hours, during an observation, Resident 34 was asleep in bed with the bilateral half
side rails elevated at the head of the bed.
On 5/14/25 at 1359 hours, Resident 34 was observed lying in bed with the bilateral half side rails elevated.
Medical record review for Resident 34 was initiated on 5/12/25. Resident 34 was admitted to the facility on
[DATE].
Review of Resident 34's Quarterly MDS assessment dated [DATE], showed Resident 34 had severe
cognitive impairment. Section GG of the assessment showed Resident 34 had impairment to both the
upper and lower extremities.
Review of Resident 34's H&P examination dated 4/10/25, showed Resident 34 is high risk for falls and had
no capacity to exercise rights and sign necessary documents therefore, family will be informed of medical
condition and/ or plan of treatment.
Review of Bed System Measurement Device Test Results Worksheet dated 5/1/25, failed to show Zones 6
and 7 were reflected and recorded on the form and assessed for the entrapment.
Cross reference to F700, example #6.
3. On 5/13/25 at 0942 hours, during an observation, Resident 40 was awake in bed with the bilateral half
side rails elevated at the head of the bed.
Medical record review for Resident 40 was initiated on 5/13/25. Resident 40 was admitted to the facility on
[DATE].
Review of Resident 40's H&P examination dated 4/11/25, showed Resident 40 had fluctuating capacity to
make decisions.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 39 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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 of Resident 40's admission MDS assessment dated [DATE], showed a BIMS score of 10 (scores of
8 to 12 suggest moderate cognitive impairment).
Review of Bed System Measurement Device Test Results Worksheet dated 5/1/25, failed to show Zones 6
and 7 were reflected and recorded on the form and assessed for the entrapment.
Residents Affected - Some
Cross reference to F700, example #7.
4. On 5/14/25 at 1127 hours, during a wound care observation, Resident 397 was awake in bed with the
bilateral half side rails elevated at the head of the bed.
Medical record review for Resident 397 was initiated on 5/12/25. Resident 397 was admitted to the facility
on [DATE].
Review of Resident 397's H&P examination dated 5/7/25, showed Resident 397 had the capacity to make
decisions.
Review of Resident 397's admission MDS assessment dated [DATE], showed a BIMS score of 15 (score of
13-15 suggests intact cognition).
Review of Bed System Measurement Device Test Results Worksheet dated 5/1/25, failed to show Zones 6
and 7 were reflected and recorded on the form and assessed for the entrapment.
On 5/15/25 at 0945 hours, an interview and concurrent record review for Residents 15, 34, 40, and 397,
was conducted with the Maintenance Supervisor. The Maintenance Supervisor acknowledged the above
findings and stated Zones 6 and 7 were not reflected on the Bed System Measurement Device Test Results
Worksheet form; therefore, the entrapment zones were inaccurately assessed.
Cross reference to F700, example #8.
5. On 5/12/25 at 0847 hours, during the initial tour, Resident 1 was lying in bed awake, oriented to name
and verbally responsive. Resident 1's bed had elevated bilateral side rails. Resident 1 stated she did not
use her side rails.
Medical record review for Resident 1 was initiated on 5/14/25. Resident 1 was admitted to the facility on
[DATE].
Review of Resident 1's H&P examination dated 4/15/25, showed Resident 1 had no capacity to understand
and make decisions.
Review of Resident 1's MDS assessment dated [DATE], showed Resident 1's cognitive skills for daily
decision-making score was 3, indicating severely impaired.
On 5/12/25 at 0856 hours, an observation and concurrent interview was conducted with CNA 2. Resident 1
was lying in bed with elevated bilateral upper side rails. CNA 2 stated Resident 1 used the bilateral upper
side rails for repositioning while in bed. CNA 2 verified the above findings.
Review of Resident 1's Bed System Measurement Device Test Results Worksheet dated 5/1/25, showed
the entrapment assessment was completed and passed for Zones 1 to 4, however, there was no
documented
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 40 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
evidence to show the facility assessed for Zones 6 and 7.
Level of Harm - Minimal harm
or potential for actual harm
Review of Resident 1's medical record failed to show for the informed consent and care plan for the use of
the bilateral upper side rails.
Residents Affected - Some
On 5/14/25 at 0909 hours, an interview was conducted with LVN 3. LVN 3 was asked who completed the
entrapment assessment. LVN 3 stated she had not heard or seen an entrapment assessment.
Cross reference to F700, example #1.
6. On 5/12/25 at 0902 hours, during the initial tour, Resident 2 was lying in bed asleep. Resident 2's bed
had elevated bilateral side rails.
Medical record review for Resident 2 was initiated on 5/14/25. Resident 2 was readmitted to the facility on
[DATE].
Review of Resident 2's MDS assessment dated [DATE], showed Resident 2's cognitive skills for daily
decision-making score was 3, indicating severely impaired.
Review of Resident 2's Bed System Measurement Device Test Results Worksheet dated 5/1/25, showed
the entrapment assessment was completed and passed for Zones 1 to 4, however, there was no
documented evidence to show the facility assessed for Zones 6 and 7.
On 5/12/25 at 0905 hours, an observation and concurrent interview was conducted with CNA 2. Resident 1
was observed lying in bed with bilateral upper side rails elevated. CNA 2 stated Resident 2 used the
bilateral upper side rails for repositioning while in bed. CNA 2 verified the above findings.
On 5/13/25 at 0837 hours, an observation and concurrent interview was conducted with LVN 5. Resident 2
was observed sitting up in bed and eating her breakfast. Resident 2's bed had elevated bilateral upper side
rails. LVN 5 verified the above findings.
Cross reference to F700, example #2.
7. On 5/14/25 at 0900 hours, an observation and concurrent interview was conducted with Resident 16.
Resident 16 was in bed, awake, alert, and verbally responsive. Resident 16's bed had elevated bilateral
upper side rails. Resident 16 stated he used the side rails for bed mobility and during transfers.
Medical record review for Resident 16 was initiated on 5/14/25. Resident 16 was readmitted to the facility
on [DATE].
Review of Resident 16's H&P examination dated 9/22/23, showed Resident 16 had the capacity to
understand and make decisions.
Review of Resident 16's MDS assessment dated [DATE], showed Resident 16's BIMS score was 15,
indicating cognitively intact.
Review of Resident 16's Bed System Measurement Device Test Results Worksheet dated 5/1/25, showed
the entrapment assessment was completed and passed for Zones 1 to 4; however, there was no
documented
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 41 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
evidence to show the facility had assessed for Zones 6 and 7.
Level of Harm - Minimal harm
or potential for actual harm
Cross reference to F700, example #3.
Residents Affected - Some
8. On 5/12/25 at 0858 hours, an initial tour observation and concurrent interview was conducted with CNA
2. Resident 19 was lying in bed, awake, alert, and eating her breakfast. Resident 19's bed had the elevated
bilateral upper side rails. CNA 2 verified the above findings. CNA 2 stated Resident 16 used the bilateral
upper side rails to reposition in bed.
Medical record review for Resident 19 was initiated on 5/14/25. Resident 19 was readmitted to the facility
on [DATE].
Review of Resident 19's MDS assessment dated [DATE], showed Resident 19's BIMS score was zero,
indicating severe cognitive impairment.
Review of Resident 19's Bed System Measurement Device Test Results Worksheet dated 5/1/25, showed
the entrapment assessment was completed and passed for Zones 1 to 4; however, there was no
documented evidence to show the facility assessed for Zones 6 and 7.
On 5/15/25 at 1009 hours, an interview, and concurrent facility document review for Residents 1, 2, 12, 16,
18, and 19 was conducted with the Maintenance Supervisor. The Maintenance Supervisor was asked about
the facility's process of their bed inspection and entrapment assessment. The Maintenance Supervisor
stated any maintenance staff could assess for entrapment using a measuring tape and document on the
Bed System Measurement Device Test Results Worksheet. Review of the Bed System Measurement
Device Test Results Worksheet for Residents 1, 2, 12, 16, 18, and 19 dated 5/1/25, showed the entrapment
assessment was completed and passed for Zones 1 to 4; however, there was no documented evidence the
facility assessed for Zones 6 and 7. The Maintenance Supervisor verified the above findings. Furthermore,
the Maintenance Supervisor stated he would rectify and update the Bed System Measurement Device Test
Results Worksheet immediately to show Zones 6 and 7.
On 5/15/25 at 1505 hours, an interview was conducted with the DON and Administrator. The DON and
Administrator were informed and acknowledged the above findings.
Cross reference to F700, example #4.
9. On 5/12/25 at 1054 hours and 5/14/25 at 0835 hours, Resident 12 was observed in bed with elevated
bilateral upper side rails.
Medical record review for Resident 12 was initiated on 5/14/25. Resident 12 was admitted to the facility on
[DATE].
Review of Resident 12's H&P examination dated 9/18/25, showed Resident 12 had no capacity to
understand and make decisions.
Review of Resident 12's Bed System Measurement Device Test Results Worksheet dated 5/1/25, showed
the entrapment assessment was completed and passed for Zones 1 to 4; however, there was no
documented evidence to show the facility assessed for Zones 6 and 7.
Cross reference to F700, example #9.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 42 of 43
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
555295
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Regents Point - Windcrest
19191 Harvard Avenue
Irvine, CA 92612
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
10. On 5/12/25 at 1045 hours and on 5/14/25 at 0835 hours, Resident 18 was observed in bed with
elevated bilateral upper side rails.
Medical record review for Resident 18 was initiated on 5/14/25. Resident 18 was admitted to the facility on
[DATE].
Residents Affected - Some
Review of Resident 18's H&P examination dated 2/8/25, showed Resident 18 did not have the capacity to
understand and make decisions.
On 5/15/25 at 1050 hours, an interview and concurrent observation was conducted with CNA 6. CNA 6
verified Resident 18 used the side rails for mobility but did not always need them.
Review of Resident 18's Bed System Measurement Device Test Results Worksheet dated 5/1/25, showed
entrapment assessment was completed and passed for Zones 1 to 4; however, there was no documented
evidence to show the facility assessed for Zones 6 and 7.
Cross reference to F700, example #10
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555295
If continuation sheet
Page 43 of 43