F 0684
Provide appropriate treatment and care according to orders, resident’s preferences and goals.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and record review, the facility failed to provide services according to the
accepted standards of clinical practice for two of 12 sampled residents (Residents 15 and 17) when:
Residents Affected - Few
1. Resident 15 did not have arm sleeves to protect his skin on the arms as ordered;
2. Resident 17's Advair HFA (an inhaler type of prescription medicine used to treat asthma) was not
administered per the manufacturer's specifications.
These failures had the potential to affect the residents' health condition and care.
Findings:
1. Review of Resident 15's physician order, dated 4/30/21, indicated arm sleeves on both upper extremities
every shift. It indicated the resident was on aspirin (an antiplatelet drug preventing platelets [a component
of the blood that stops bleeding] from clumping together to form a clot) daily.
During an observation on 3/8/22 at 12:25 p.m. and 3/9/22 at 7:30 a.m., Resident 15 had multiple skin
discolorations and a skin tear on both arms and hands. The resident was not wearing arm sleeves.
During an observation and concurrent interview on 3/11/22 at 12:30 p.m., certified nursing assistant B
(CNA B), who was involved in Resident 15's care, stated the resident did not wear arm sleeves and did not
have them.
2. During a medication pass observation on 3/9/22 at 8:01 a.m., licensed vocational nurse C (LVN C)
administered Resident 17's Advair HFA. After administering the first puff (inhalation), the resident did not
close her mouth to hold her breath and breathe in. She started breathing out after getting the first puff. LVN
C did not instruct the resident to hold her breath and breathe in. After five seconds, LVN C administered the
second puff to the resident.
During an interview on 3/9/22 at 1:39 p.m., LVN C stated the wait time should be three to five minutes
between inhalations.
Review of the facility's policy, Oral Inhalations, dated 5/2016, indicated, Hold breath for 5-10 seconds or as
long as possible to allow medication to reach deeply into lungs, slowly exhale . if another puff of the same
or different medication is required, follow the manufacturer's product information for administration
instructions including the acceptable wait time between inhalations.
(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 10
Event ID:
055311
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
Level of Harm - Minimal harm
or potential for actual harm
Review of the manufacturer's package insert, dated 2/2021, indicated, After the spray comes out .take the
inhaler out of your mouth and close your mouth .Hold breath for about 10 seconds or for as long as is
comfortable. Breathe out slowly .wait about 30 seconds and shake the inhaler well for 5 seconds. Repeat
the steps .
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 2 of 10
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
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** 2. Review of
Resident 15's care plans indicated the resident was at high risk for falls related to history of falls, confusion,
gait, and balance problems.
Review of Resident 15's clinical records indicated the resident had fall incidents on 1/18/21, 3/3/21,
10/12/21, 1/2/22, 1/24/22, 2/6/22, and 2/18/22.
Review of Resident 15's IDT Fall Review, dated 1/19/21, indicated the IDT reviewed the resident's 1/18/21
fall incident and the IDT did not recommend any new interventions or revise the current interventions to
prevent falls.
Review of Resident 15's IDT fall review, dated 1/26/22, indicated the IDT reviewed the resident's 1/24/22 fall
incident and one of the recommendations was to take the resident to assess for bathroom privileges after
lunch.
Review of Resident 15's IDT fall review, dated 2/8/22, indicated the IDT reviewed the resident's 2/6/22 fall
incident and there was no new recommendation to prevent recurrent falls.
During an interview on 3/10/22 at 12:19 p.m., the director of nursing (DON) and the SD, who participated in
Resident 15's IDT meetings, stated after fall incidents, the IDT reviewed each fall incident and made
recommendations to prevent recurrent falls. DON and the SD reviewed Resident 15's clinical records and
confirmed that there were no new or revised recommendations for fall incidents on 1/19/21 and 2/8/22. The
SD stated on 1/26/22, the IDT planned to assess the resident's toileting after lunch, but the plan was not
communicated to the certified nursing assistants (CNAs) and there was no evidence the recommendation
was implemented.
Review of the facility's policy, Resident Falls Management, dated 11/2016, indicated after implementation of
the plan, subsequent incidence of falls is followed by reevaluations, which includes discussion of possible
interventions needed to prevent further recurrence.
Based on observation, interview, and record review, the facility failed to provide a safe environment for
three of 12 sampled residents (Residents 2, 15, and 23) when:
1. The interdisciplinary team (IDT, team of diverse caregivers involved in the treatment plan for the resident)
recommendations were not implemented for Residents 2 and 15;
2. The IDT did not initiate or revise interventions to prevent recurrent falls for Resident 15; and
3. Resident 23's fall assessment was missing upon admission.
These had the potential to result in falls and injuries to the residents.
Findings:
1. Review of Resident 2's clinical record indicated she had diagnoses including Parkinson's disease (a
disease that include symptoms of slowness of movements, muscle rigidity, involuntary
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 3 of 10
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
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
tremors/shaking and impaired balance and posture) and hypertension (high blood pressure).
Level of Harm - Minimal harm
or potential for actual harm
Review of Resident 2's Morse Fall Scale (a method of assessing a person's likelihood of falling), dated
4/13/21 indicated Resident 2 was a high risk for falls.
Residents Affected - Few
Review of Resident 2's IDT Fall Review, dated 8/16/21 indicated Resident 2 fell on 8/13/21. Resident 2 was
found kneeling next to her bed. The IDT conclusions indicated staff will perform frequent rounding to assist
resident with bathroom privilege, thirst or hunger.
Review of Resident 2's IDT Fall Review, dated 12/29/21 indicated Resident 2 fell on [DATE]. Resident 2 was
found sitting on the floor in her room. The IDT conclusions indicated the following: urinalysis (UA, a urine
test that can check for infection or kidney problems) and culture and sensitivity (C&S, culture is a test to
identify the bacteria causing an infection and sensitivity was used to identify which antibiotic can be used to
treat the infection) as ordered; anticipate needs every shift; and reorientation as needed.
Review of Resident 2's Lab Results Report, dated 1/1/22 indicated, NO UA RCVD [received] FOR UA C&S
and RECOLLECT. There was no documentation that indicated the reason Resident 2's urine was not
collected.
During an interview on 3/10/22 at 1:15 p.m., the minimum data set coordinator (MDSC) stated the nurse
assigned to Resident 2 should have collected a urine sample to send to the lab. The MDSC confirmed there
were no other UA C&S results in Resident 2's chart.
During an interview on 3/11/22 9:51 a.m., the staff developer (SD) stated there was no documentation that
indicated staff frequently performed rounding to assist Resident 2. The SD stated staff are already
anticipating Resident 2's needs and it was not a new intervention.
3. Review of Resident 23's face sheet indicated Resident 23 was an [AGE] year old female admitted on
[DATE] with admitting diagnoses of generalized muscle weakness, chronic obstructive pulmonary disease
(COPD, lung disease that blocks airflow making it hard to breathe), and diabetes mellitus type two
(DM,chronic condition that affects the way the body processes sugar with the body not making enough
insulin or being resistive to it).
During record review and concurrent interview with the SD on 3/10/22 at 12:39 p.m., the SD confirmed the
Morse falls risk assessment was missing for Resident 23 upon admission. The SD confirmed the Morse
falls risk assessment should have been completed on admission.
Record review of the facility's policy titled Fall Evaluation (MORSE Scale) and Management, revised
February 2000, indicated the licensed nurse should complete the Morse falls risk assessment on admission
and based on that score determine if the resident is at a low risk, a moderate risk, or a high risk for falls.
Per policy, appropriate care plan interventions should be developed based on the assessed risk level.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 4 of 10
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
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 0690
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide appropriate care for residents who are continent or incontinent of bowel/bladder, appropriate
catheter care, and appropriate care to prevent urinary tract infections.
Based on observation, interview, and record review, the facility failed to ensure nursing staff assessed one
of 12 sampled residents (Resident 7) for removal of an indwelling catheter (a tube inserted into the bladder
to drain urine). This failure had the potential for the resident to have an unnecessary indwelling catheter
with increased risk of catheter related complications i.e., infection.
Findings:
During an observation on 3/8/22 at 9:14 a.m., Resident 7 had an indwelling catheter with a drainage bag.
Review of Resident 7's Nursing Progress Notes, dated 2/19/22, indicated the resident was transferred to an
acute care hospital for respiratory failure.
Review of Resident 7's Discharge Summary from the acute care hospital, dated 2/21/22, indicated the
resident was discharged with the indwelling catheter.
Review of Resident 7's CARE CONFERENCE, dated 2/23/22, indicated on 2/21/22, the resident was
readmitted to the facility.
During a record review and concurrent interview, on 3/10/22 at 12:37 p.m., the director of nursing (DON)
reviewed Resident 7's clinical records and stated there was no documented evidence the staff assessed
whether the resident's indwelling catheter was necessary upon admission.
Review of the facility's policy, Evaluation for Indwelling Catheters, dated 2/2018, indicated, Residents
admitted with indwelling catheters have them removed when there is no valid medical justification, and
Each resident is evaluated at admission .for indwelling catheter usage .when possible, discontinue the
indwelling catheter usage and initiate toileting/retraining evaluation protocol as appropriate. Resident
admitted with an indwelling catheter not meeting the clinical conditions . have catheter usage discontinued
within 3 to 5 days as appropriate per physician order.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 5 of 10
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
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 0712
Ensure that the resident and his/her doctor meet face-to-face at all required visits.
Level of Harm - Minimal harm
or potential for actual harm
Based on interview and record review, the facility failed to ensure an attending physician visited and
evaluated one of 12 sampled residents (Resident 8) in a timely manner. This failure had the potential to
delay identifying the resident's medical needs and providing necessary care and treatment appropriately.
Residents Affected - Few
Findings:
Review of Resident 8's Physician Notes indicated the resident was seen by the attending physician on
9/8/21.
During an interview on 3/11/22 at 8:19 a.m., the director of nursing (DON) stated the resident did not like
her attending physician, the facility found another physician, and the new attending physician would start
providing services for Resident 8. The DON stated the Medical Record staff (MR) monitors the physicians'
progress notes indicating the physicians visit the residents on a regular basis.
During an interview on 3/11/22 at 12:35 p.m., the MR stated she did not monitor if the physicians visited the
residents and made their progress notes.
During a phone interview on 3/11/22 at 1:20 p.m., Resident 8's attending physician (AP A) stated the
resident refused to have AP A come into her room and she could not assess the resident. AP A stated
September 2021 was her last visit to see the resident and complete a physical examination.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 6 of 10
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
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 0757
Ensure each resident’s drug regimen must be free from unnecessary drugs.
Level of Harm - Minimal harm
or potential for actual harm
2. Review of Resident 15's physician order, dated 1/31/22, indicated the resident was on Seroquel (an
antipsychotic medicine to treat schizophrenia [a serious mental illness that interferes with a person's ability
to think clearly, manage emotions, make decisions and relate to others]).
Residents Affected - Few
Review of Resident 15's AIMS assessment indicated it was done on 7/1/20, 2/17/21 and 9/7/21.
During an interview on 3/10/22 at 9:42 a.m., the director of social service (DSS) reviewed Resident 15's
clinical records and stated the resident had taken Seroquel since 2020.
During an interview on 3/11/22 at 11:10 a.m., the staff developer (SD) stated the staff assess the residents
who take antipsychotic medications, completing AIMS quarterly when their comprehensive care plans are
reviewed. SD stated Resident 15's AIMS assessment was not done quarterly.
During record review of the facility's policy Psychotropic Drugs, updated January 2019, indicated
monitoring for appropriate diagnosis of behavioral symptoms and monitoring for any side effects of the drug
that may be considered unnecessary.
Based on interview and record review, the facility failed to ensure adequate monitoring of psychotropic
medications for two of 12 sampled residents (Residents 5 and 15) when the side effects of Ambien
(medication used to treat insomnia, a sleep disorder) were not monitored for Resident 5 and the Abnormal
Involuntary Movement Scale (AIMS, test to monitor movement disorders in a person taking an antipsychotic
medication) assessment was not completed for Resident 15. These failures had the potential to result in
unnecessary medications.
Findings:
Review of Resident 5's clinical record indicated he had diagnoses including cervical disc disorder (changes
in the cervical [neck] part of the spine, resulting in pain, tingling, or numbness) with telepathy (injury to the
spinal cord).
Review of Resident 5's physician orders indicated he had an order for Ambien tablet 10 milligrams (mg, unit
of measurement) give 10 mg by mouth every 24 hours as needed for insomnia, dated 3/5/22. Resident 5
also had discontinued order for Ambien tablet 10 mg give 10 mg by mouth every 24 hours as needed for
insomnia, dated 2/18/22.
Review of Resident 5's medication administration record (MAR, record of medications given), dated
February 2022 indicated Ambien 10 mg was given each day from 2/18/22 to 2/28/22.
Review of Resident 5's MAR, dated March 2022 indicated Ambien 10 mg was given on 3/1/22, 3/2/22,
3/6/22, 3/7/22, and 3/8/22. There was no documentation that indicated side effects of Ambien were
monitored for Resident 5 in February 2022 and March 2022.
During an interview on 3/09/22 at 21:25 p.m., the minimum data set coordinator (MDSC) confirmed there
was no side effect monitoring for Resident 5 in February and March 2022. The MDSC stated side effects of
Ambien should be monitored.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 7 of 10
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Implement gradual dose reductions(GDR) and non-pharmacological interventions, unless contraindicated,
prior to initiating or instead of continuing psychotropic medication; and PRN orders for psychotropic
medications are only used when the medication is necessary and PRN use is limited.
Based on interview and record review, the facility failed to ensure two of 12 sampled residents (Residents 6
and 11) had gradual dose reduction (GDR) attempts for their psychotropic medications (drugs that affects
brain activities associated with mental processes and behavior). This failure resulted in the residents not
having the opportunity to be free from the unnecessary psychotropic medications.
Findings:
1. Review of Resident 6's Note to Attending Physician/Prescriber, dated 9/15/21, indicated the resident had
been taking the antidepressant, paroxetine (antidepressant medication), 20 milligrams (mg) once a day and
the consultant pharmacist recommended gradual dose reduction (GDR). Resident 6's attending physician
(AP A) responded by checking, Resident with good response, maintain the current dose. The form's section
for the attending physician/prescriber to indicate clinical rationale for continuing medication dosage was
blank.
During a record review and concurrent interview with the director of social service, on 3/10/22 at 9:47 a.m.,
the DSS reviewed Resident 6's clinical record and stated there was no documented clinical rationale to
continue the current dose of paroxetine.
During a phone interview on 3/11/22 at 1:30 p.m., AP A stated she did not document a clinical rationale to
continue Resident 6's paroxetine dose.
2. Review of Resident 11's physician order, dated 9/13/21, indicated the resident's target behaviors
(behaviors monitored by the staff for the use of psychotropic medications) were unhappiness as evidenced
by sad facial expression. Resident 11's associated triggers were missing family/home and wanting to be
with his family.
Review of Resident 11's physician order, dated 9/24/21, indicated Celexa (a medication for the treatment of
depression) 20 mg at bedtime.
Review of Resident 11's Note to Attending Physician/Prescriber, dated 1/26/22, indicated a consultant
pharmacist reviewed the resident's drug regimen and recommended gradual dose reduction (GDR) for
Celexa. The attending physician declined by checking, Resident with good response, maintain the current
dose. The form's section for the attending physician/prescriber to indicate clinical rationale for continuing
medication dosage was blank.
During a record review and concurrent interview with the DSS on 3/9/22 at 2:49 p.m., the DSS stated
Resident 11's Celexa was initiated on 7/6/21. She reviewed target behavior monitoring sheets, from 8/2021
to 2/2022, and stated the resident had not shown any behaviors. The DSS reviewed Resident 11's clinical
records and stated there was no documented clinical rationale to continue the current dose.
During a phone interview with AP A, on 3/11/22 at 1:20 p.m., Resident 11's AP A stated she did not
document a clinical rationale to continue the current dose of Celexa.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 8 of 10
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0758
Level of Harm - Minimal harm
or potential for actual harm
During record review of the facility's policy Psychotropic Drugs, updated January 2019, indicated the GDR
consists of tapering the resident's daily dose determine if the resident's symptoms can be controlled by a
lower dose of medication. The policy indicated the physician should a provide a justification including
clinical appropriateness for continued medication use/dose.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 9 of 10
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
055311
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/11/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Katherine Healthcare
315 Alameda Avenue
Salinas, CA 93901
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 0912
Level of Harm - Potential for
minimal harm
Residents Affected - Some
Provide rooms that are at least 80 square feet per resident in multiple rooms and 100 square feet for single
resident rooms.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based
interview and record review, the facility failed to ensure rooms [ROOM NUMBER] had at least 80 square
feet per resident. Having less than 80 square feet per resident could potentially compromise the care and
services the residents receive in the facility.
Findings:
Review of the facility's Client Accommodations Analysis indicated rooms [ROOM NUMBER] were approved
for two beds and measured 74.25 square feet per resident, 78.48 square feet per resident, and 76.30
square feet per resident respectively.
During the survey, there were no concerns from residents and staff regarding room size.
Continuance of the room waiver is recommended.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055311
If continuation sheet
Page 10 of 10