F 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to maintain an accurate reconciliation of the controlled
medication that had been administered for two of three sampled residents (Residents 2 and 3).
This failure increased the risk for medication error, which could negatively impact the residents' health
condition.
Findings:
A review of Resident 2's admission Record, indicated the resident was admitted to the facility on [DATE],
with diagnoses which included fracture (break in the bone) of right humerus (upper arm bone).
A review of Resident 2 ' s Physician Order Report, for May 2025, indicated, oxycodone (narcotic
medication) - Schedule II tablet; 5 mg (milligram-unit of measurement); amt (amount): 1 tab; oral Special
Instructions: Dx (diagnosis) Moderate pain 5-6 (pain level), Severe pain 7-10 (pain level) Every 4 (four)
Hours - PRN . Further review of the physician order report indicated the medication was ordered on May 2,
2025.
On May 29, 2025, at 10:20 a.m., during an interview, Licensed Vocational Nurse (LVN) 1 stated when
administering narcotics, the nurses are expected to sign on the narcotic sheet that they removed the
medication and then sign the Medication Administration Record (MAR) after administering the medication.
During a concurrent review of Resident 2' s narcotic sheet and electronic MAR for May 2025, LVN 1 stated
Resident 2' s Oxycodone was removed from the medication cart on the following dates and times:
a. May 6, 2025, at 8:39 a.m., and 8:45 p.m.;
b. May 7, 2025, at 6:50 a.m. and 11:30 a.m.;
c. May 8, 2025, at 9:34 a.m.; and
d. May 11, 2025, at 11:54 p.m.
LVN 1 stated oxycodone was not documented in the MAR as administered on May 6, May 7, May 8, and
May 11, 2025. LVN 1 stated the licensed nurses should sign the MAR that they administered the
medication.
(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 4
Event ID:
056229
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
056229
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/29/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Palm Springs Healthcare & Rehabilitation Center
277 S Sunrise Way
Palm Springs, CA 92262
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
A review of Resident 3's admission record, indicated the resident was initially admitted to the facility on
[DATE], and was re-admitted on [DATE], with diagnoses which included urinary tract infection.
A review of Resident 3's Physician Order Report, for May 2025, indicated, acetaminophen-hydrocodone
(Norco - narcotic) 325-5 mg tablet; 5/325 MG; amt: 1 tab; oral Special Instructions: PRN Moderate pain
(SCALE 5-6) OR Severe pain (SCALE 7-10) .Every 4 Hours - PRN . The physician order report indicated
the medication was ordered on April 9, 2025.
On May 29, 2025, at 11:07 a.m., during an interview and record review of Resident 3 ' s narcotic sheet and
electronic MAR for May 2025, the Infection Preventionist (IP) stated, Resident 3 ' s Norco was removed
from the medication cart on May 1, 2025, at 4:35 p.m., on May 13, 2025, at 12:47 p.m., and May 14, 2025,
at 8:57 a.m., but was not documented on the MAR as administered. The IP stated the practice was when
narcotics were given, the licensed nurses should be signing the MAR.
On May 29, 2025, at 2:15 p.m. during an interview, the Director of Nursing (DON) stated the licensed
nurses should sign the narcotic sheet and the MAR when they administer narcotic medications. The DON
stated the facility policy for Controlled Substances should be followed.
On May 29, 2025 at 3:40 p.m., during a concurrent interview with LVN 2 and a record review of Residents 2
and 3's narcotic sheet and MAR, LVN 2 stated he would document narcotics administration on the narcotic
sheet and on the MAR. LVN 2 stated he administered Resident 3's Norco on May 1, 2025 and Resident 2's
oxycodone on May 6, 2025, but he did not document on the MAR. LVN 2 stated he probably got busy and
he should have documented on Residents 2 and 3's MAR.
A review of the facility policy and procedure titled, Controlled Substances, dated November 2017, indicated
.Controlled Medications are . medications are subject to special handling, storage, disposal, and record
keeping at the nursing care center, in accordance with federal and state laws and regulations . When a
controlled medication is administered, the licensed nurse administering the medication immediately enters
the following information on the accountability record when removing dose from controlled storage .Date
and time of administration .Amount administered .Signature of the nurse administering the dose .Administer
the controlled medication and document dose administration on the MAR .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056229
If continuation sheet
Page 2 of 4
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
056229
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/29/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Palm Springs Healthcare & Rehabilitation Center
277 S Sunrise Way
Palm Springs, CA 92262
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to implement proper infection control precaution
in accordance with the facility policy and procedure, when one of nine residents (Resident 1) was identified
positive of carbapenem-resistant pseudomonas aeruginosa (CRPA - a type of bacteria resistant to a
powerful class of antibiotics) on March 28, 2025.
Residents Affected - Few
This failure had the potential to negatively impact the vulnerable residents in the subacute care (a level of
care needed by a resident who does not require hospital acute care but who requires more intensive
licensed skilled nursing care than is provided to the majority of patients in a skilled nursing facility) unit.
Findings:
A review of Resident 1's admission record indicated the resident was initially admitted in the facility on
September 28, 2024, and re-admitted on [DATE], with diagnoses which included respiratory failure with
tracheostomy (an opening surgically created through the neck into the windpipe to allow air to fill the lungs)
and resistance to carbapenems (occurs when bacteria defeat the antibiotic designed to kill them).
A review of Resident 1's Sputum Culture, Final Update Result, dated March 28, 2025, indicated there was
heavy growth of CRPA. A review of the same document indicated that the medical doctor (MD) was notified
and ordered no antibiotics and for the staff to monitor.
On May 28, 2025, at 12:15 p.m., during observation, there was contact precaution (used to prevent the
spread of infections transmitted through direct or indirect contact with a patient or environment) and droplet
precaution (used to prevent the spread of diseases that are transmitted through respiratory droplets
generated by an infected individual when coughing and sneezing) signs posted outside the door of
Resident 1' s room. Resident 1 was lying in bed, turned to his left side, with tracheostomy connected to
oxygen.
On May 28, 2025, at 1:20 p.m., during an interview, Registered Nurse (RN) 1 stated on March 16, 2025, the
resident had a fever and sputum culture was ordered and an antibiotic therapy was started. RN 1 stated the
facility received the final sputum culture result on March 28, 2025, which indicated heavy growth of CRPA.
RN 1 stated it was another RN who received the results. RN 1 stated there was no documentation in the
progress notes that the RN notified the Infection Preventionist (IP) on Resident 1 ' s sputum culture result.
RN 1 stated the IP should be notified when a resident ' s laboratory result indicated CRPA.
On May 28, 2025, at 1:35 p.m., during an interview, the IP stated on April 22, 2025, RN 2 reported Resident
2 ' s sputum culture result which came out positive of CRPA on March 28, 2025. The IP stated she moved
Resident 1 to a different room and placed the resident on contact and droplet precaution. The IP stated she
did not receive any report that Resident 1 had CRPA before April 22, 2025. The IP stated Resident 1 should
have been placed on contact isolation immediately on March 28, 2025. The IP stated contact isolation
required for the staff to don PPE (Personal Protective Equipment) every time they would enter the residents
' room regardless of what they are going in for and residents have dedicated equipment such as blood
pressure machine and stethoscope. The IP stated CRPA required contact isolation.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056229
If continuation sheet
Page 3 of 4
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
056229
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/29/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Palm Springs Healthcare & Rehabilitation Center
277 S Sunrise Way
Palm Springs, CA 92262
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
On May 28, 2025, at 4:19 p.m., during an interview, the Director of Nursing (DON) stated the facility
received Resident 1's sputum culture result but was not reviewed. The DON stated nothing was
implemented until April 22, 2025. The DON stated the RN did not notify the IP when she received Resident
1's sputum culture. In addition, the DON stayed the RN should have reported the culture result to the IP and
to the physician and document it.
Residents Affected - Few
On May 29, 2025, at 11:25 a.m., during an interview, the IP stated Resident 1 was not on contact isolation
for a month.
A review of the undated facility policy and procedure titled, Carbapenem Resistant Pseudomonas
Aeruginosa (CRPA), indicated, .The facility will adhere to the Centers for Disease Control and Prevention
(CDC) guidelines for the surveillance, diagnosis, and treatment of Carbapenem-resistant Pseudomonas
Aeruginosa (CRPA) . The facility will adhere to the CDC's recommendations to prevent CRPA transmission
.Contact Precautions: Place CRPA colonized or infected residents on Contact Precautions (CP) .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056229
If continuation sheet
Page 4 of 4