F 0554
Allow residents to self-administer drugs if determined clinically appropriate.
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 ensure the interdisciplinary team (IDT)
assessed and documented for Resident 49 being capable of self-administering medications, prior to having
the medication stored at the resident's bedside for administering it himself.
Residents Affected - Few
This had the potential for inadequate drug therapy by allowing the resident to administer doses below or
above the prescribed dose by the physician.
Findings:
On January 10, 2024, at 2:10 p.m., during inspection of the medication cart located in Red Hall, there was
a manufacturer box for albuterol (medication to treat difficulty in breathing) aerosol inhaler, which had a
pharmacy label to indicate it belonged to Resident 49, without the inhaler inside, stored in the bottom
drawer of the cart.
In a concurrent interview, the Licensed Vocational Nurse (LVN) 1 stated the albuterol inhaler was kept at the
resident's bedside inside the resident's room for resident to self-administer the medication.
LVN 1 stated there was no order for the resident to keep the medication at bedside for self-administration.
On January 10, 2024, at 2:35 p.m., it was noted the inhaler was stored in the drawer of the side table next
to the resident's bed. The inhaler was not labeled to indicate it belonged to Resident 49.
In a concurrent interview, the Infection Preventionist (IP) stated there was no self-administration of
medication for the resident done by the Interdisciplinary Team (IDT).
On January 10, 2024, medical record of Resident 49 was reviewed, and the following was noted:
The resident was admitted on [DATE], with diagnoses that included asthma (condition that causes difficulty
in breathing);
There was a physician order on December 4, 2023, for albuterol sulfate aerosol inhaler 108 microgram per
actuation with the direction to inhale two puffs by mouth every six hours for shortness of breath; and
The electronic medication administration record (eMAR) of the resident for January 2024, indicated
(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 19
Event ID:
555775
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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 0554
the medication was administered daily every six hours.
Level of Harm - Minimal harm
or potential for actual harm
The facility's policy and procedure titled, Administering Medications, revised, April 2019, was reviewed and
it indicated:
Residents Affected - Few
.Residents may self-administer their own medications only if the Attending Physician in conjunction with the
Interdisciplinary Care Planning Team, has determined that they have the decision-making capacity to do so
safely .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 2 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0655
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Create and put into place a plan for meeting the resident's most immediate needs within 48 hours of being
admitted
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to develop a care plan for one of one resident
reviewed for oxygen use (Resident 16) and for one of three residents reviewed for edema [swelling]
(Resident 165).
This failure had the potential to negatively impact the residents' quality of care and had the potential for
staff to not be aware of the residents' care needs and provide appropriate treatment.
Findings:
1. On January 8, 2024, at 11:53 a.m., Resident 16 was observed in bed, with oxygen (O2) via nasal
cannula (NC - a tube used to deliver oxygen through the nose). Resident 16's oxygen administration was
observed at three liters per minute (LPM).
In a concurrent interview, Resident 16 stated she uses O2 continuously due to shortness of breath and she
takes it off at times during the day.
Resident 16's record was reviewed. Resident 16 was admitted to the facility on [DATE], with diagnoses
which included chronic obstructive pulmonary disease (COPD - a disease that causes obstructed airflow).
The physician's order dated January 4, 2024, indicated, .Oxygen Therapy Continuous - 2 Liters Per/Minute
Via Nasal Cannula. May Titrate Oxygen Up to 5 Liters To Maintain O2 Sats > 90% every shift for (SOB
[short of breath] Related: COPD) .
On January 10, 2024, at 9:03 a.m., a concurrent interview and record review was conducted with Licensed
Vocational Nurse (LVN) 1. LVN 1 stated Resident 16 had a physician's order for oxygen. In a concurrent
review of Resident's 16's record, LVN 1 stated there was no documentation a care plan for oxygen was
initiated for Resident 16. LVN 1 stated Resident 16 should have had a care plan for oxygen administration.
On January 10, 2024, at 9:20 a.m., the Director of Nursing (DON) was interviewed. The DON confirmed a
care plan for oxygen administration for Resident 16 was not initiated. The DON stated a care plan for O2
administration should have been developed for Resident 16.
2. During a concurrent observation and interview, on January 8, 2024, at 12:55 p.m., with Resident 165 in
her room, Resident 165 was observed lying in bed awake, alert, and able to verbalize her needs. Resident
165 was observed wearing a left arm compression sleeve (a type of medical garment used to increase
blood flow, reduce pain and swelling). Resident 165 was observed with some edema (swelling) of her left
hand.
Resident 165 stated she had a history of lymphedema (a condition caused by a blockage in the lympahatic
system, part of immune and circulatory system) for five years. She stated she had a history of breast
cancer, and sometimes the edema was bad.
During a review of Resident 165's record, Resident 165 was admitted to the facility on [DATE], with
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 3 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0655
diagnoses which included fracture of fourth lumbar vertebra (bones in the spine).
Level of Harm - Minimal harm
or potential for actual harm
The nursing notes dated January 3, 2024, entered at 10:39 p.m., indicated, .Resident noted to have edema
to left upper extremity. Encourage elevation. Resident stated she has edema due to (d/t) history of breast
cancer to left breast .
Residents Affected - Few
The nursing progress notes from January 4, 2024 to January 8, 2024, did not indicate licensed nurse
observation and monitoring of Resident 165's left arm edema and the presence of the left arm compression
sleeve.
The initial social service evaluation dated January 4, 2024, indicated Resident 165 was alert and oriented
to person, place, time, and situation.
The baseline care plans upon admission did not include the identified assessment of edema on Resident
165's left upper extremity.
During a concurrent observation and interview, on January 9, 2024, at 9:05 a.m., with Resident 165,
indicated Resident 165 was awake, alert, and able to verbalize her needs. Resident 165's left hand was
observed without edema. She stated she felt better having no swelling on her left arm. She stated she wore
her compression sleeve all day and all night.
During a concurrent observation and interview, on January 9, 2024, at 9:45 a.m., conducted with the
Director of Nursing (DON) in the resident's room, the DON acknowledge Resident 165 was wearing a left
arm compression sleeve.
During a concurrent interview and record review, on January 9, 2024, at 10:05 a.m., with the DON, the
nurse's notes from January 3, 2024 to January 9, 2024, were reviewed. The DON confirmed on January 3,
2024, the licensed nurse documented Resident 165 had edema on her left upper extremity. The DON
stated there were no further monitoring and assessments of Resident 165's edema on every shift after
January 3, 2024. The DON further stated there was no assessment of Resident 165's compression sleeve.
A review of Resident 165's care plans indicated there was no documented evidence the baseline care plan
for Resident 165's edema and compression sleeve was developed.
The DON stated the licensed nurse who admitted Resident 165 should have initiated the baseline care plan
for Resident 165's edema of her left upper extremity. He stated there was no physician's order for the
compression sleeve. He stated the physician should have been contacted by the licensed staff.
During a concurrent observation and interview, on January 10, 2024, at 10:30 a.m., Resident 165 was
observed lying in bed, awake, alert, and able to verbalize her needs. Resident 165 stated she just returned
from physical therapy. Resident 165 was observed with her left arm compression sleeve on and without
edema on the left hand.
The facility's policy and procedure titled, Care Plans - Baseline, dated December 2016, was reviewed. The
policy indicated, .A baseline plan of care to meet the resident's immediate needs shall be developed for
each resident within forty eight (48) hours of admission .The baseline care plan will be used until the staff
can conduct the comprehensive assessment and develop an interdisciplinary
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 4 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0655
person-centered care plan .
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 5 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to implement the care plan in using the dignity
bag for resident's indwelling urinary catheter (catheter used to drain urine from the bladder into a bag
outside the body) drainage bag for one of one resident reviewed (Resident 164).
This failure resulted in Resident 164's indwelling urinary catheter drainage bag's urine being visibly
exposed to visitors entering the room and the drainage bag did not have protection from contact with the
bed and other equipment at the resident's bedside.
Findings:
On January 8, 2024, at 12:25 p.m., Resident 164 was in a room designated with contact isolation
precautions (steps healthcare facility visitors and staff need to follow before going into a patient's room to
stop germs from spreading by touching the patient or surfaces in the room). The personal protective
equipment (PPE - used to minimize exposure to hazards that cause serious illnesses) cart was observed
outside the room.
During a concurrent observation and interview on January 8, 2024, at 12:28 p.m., with Resident 164 in his
room, Resident 164 was observed lying in bed awake, alert, and able to verbalize his needs.
Resident 164 stated he had infected wounds on his right foot.
A wound vac (device used to remove excess fluid and promote healing of the wounds) was observed on
resident's right side of his foot dressing.
Resident 164 was observed with an indwelling urinary catheter attached to a drainage bag containing
yellow urine. The indwelling urinary catheter drainage bag's bottom was touching the floor. The drainage
bag was uncovered.
During a concurrent observation and interview on January 8, 2024, at 12:30 p.m., with the Director of
Nursing (DON), in Resident 164's room, the DON stated the resident's indwelling urinary catheter drainage
bag was on the floor. He stated the drainage bag should not be touching the floor and should be covered
with the dignity bag.
During a concurrent observation and interview on January 8, 2024, at 12:40 p.m., with the Infection
Preventionist (IP) in Resident 164's room, the IP stated the indwelling urinary catheter drainage bag should
not be touching the floor and should be covered with the dignity bag.
On January 8, 2024, Resident 164's record was reviewed. Resident 164 was admitted to the facility on
[DATE], with diagnoses which included End Stage Renal Disease (ESRD - kidney disease), and acute
Osteomyelitis (bone infection)) of right ankle and foot, and recent right amputation of second and third toes
with Methicillin Resistant Staphylococcus Aureus (MRSA - a serious infection that can lead to sepsis or
death).
During a review of Resident 164's record, indicated a care plan for indwelling urinary catheter, with goal
and interventions. The care plan indicated, .Place indwelling urinary catheter bag in
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 6 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0656
dignity/privacy bag .
Level of Harm - Minimal harm
or potential for actual harm
On January 10, 2024, at 10:23 a.m., a concurrent interview and record review was conducted with the
DON. The DON reviewed Resident 164's care plan for indwelling urinary catheter. The care plan indicated a
goal and interventions which included .Place indwelling urinary catheter bag in dignity/privacy bag .
Residents Affected - Few
The DON acknowledged the care plan intervention of placing the indwelling urinary catheter drainage bag
in dignity/privacy bag was not followed.
The facility's policy and procedure titled, Care Plans, Comprehensive Person - Centered, dated December
2016, was reviewed. The policy indicated, .A comprehensive, person-centered care plan that includes
measurable objectives and timetables to meet the resident's physical, psychosocial and functional needs is
developed and implemented for each resident .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 7 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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 0658
Ensure services provided by the nursing facility meet professional standards of quality.
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 notify the physician of resident's left upper
extremity edema and the compression sleeve, for one of one resident reviewed (Resident 165).
Residents Affected - Few
This failure had potential to affect Resident 165's blood circulation on her left upper extremity and can lead
to skin breakdown and other complications.
Findings:
During concurrent observation and interview, on January 8, 2024, at 12:55 p.m., with Resident 165 in her
room, Resident 165 was observed lying in bed awake, alert, and able to verbalize her needs. Resident 165
was observed wearing a left arm compression sleeve (a type of medical garment used to increase blood
flow, reduce pain and swelling). Resident 165 was observed with edema (swelling) of her left hand.
Resident 165 stated she had a history of lymphedema (a condition caused by a blockage in the lympahatic
system, part of immune and circulatory system) for five years. She stated she had a history of breast
cancer. She stated sometimes the edema was bad.
Resident 165's record was reviewed. The record indicated Resident 165 was admitted to the facility on
[DATE], with diagnoses which included fracture of fourth lumbar vertebra (bone in the spine).
The nursing notes dated January 3, 2024, entered at 10:39 p.m., indicated, .Resident noted to have edema
to left upper extremity. Encourage elevation. Resident stated she has edema due to (d/t) history of breast
cancer to left breast .
The physician's orders dated January 3, 2024, indicated there was no specific orders for monitoring of
Resident 165's edema of left upper extremity and instructions for the care of compression sleeve.
The nursing progress notes from January 4, 2024 to January 8, 2024, did not indicate licensed nurse
observation and monitoring of Resident 165's left arm edema and the presence of the left arm compression
sleeve.
During a concurrent observation and interview, on January 9, 2024, at 9:05 a.m., with Resident 165,
Resident 165 was awake, alert, and able to verbalize her needs. Resident 165's left hand was observed
without edema. She stated she felt better having no swelling on her left arm. She stated she wore her
compression sleeve all day and all night.
During a concurrent observation and interview, on January 9, 2024, at 9:45 a.m., conducted with the
Director of Nursing (DON) in Resident 165's room, the DON acknowledge Resident 165 was wearing a left
arm compression sleeve.
During a concurrent interview and record review, on January 9, 2024, at 10:05 a.m., with the DON, the
nurse's notes from January 3, 2024 to January 9, 2024, were reviewed. The DON confirmed on January 3,
2024, the licensed nurse documented Resident 165 had edema on her left upper extremity. The DON
stated there were no further monitoring and assessments of resident's edema on every shift after
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 8 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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 0658
January 3, 2024. The DON stated there was no assessment of Resident 165's compression sleeve.
Level of Harm - Minimal harm
or potential for actual harm
A review of the physician's orders from January 3, 2024 to January 9, 2024, indicated there was no
physician's order for monitoring of Resident 165's edema every shift and compression sleeve instructions.
Residents Affected - Few
The DON stated the licensed nurse who admitted Resident 165, should have informed the physician
regarding Resident 165's edema of the left upper extremity and the resident's compression sleeve. He
stated there was no physician's order for the compression sleeve, and the monitoring of resident's left
upper extremity edema.
During a concurrent observation and interview, on January 10, 2024, at 10:30 a.m., Resident 165 was
observed lying in bed, awake, alert, and able to verbalize her needs. Resident 165 stated she just returned
from physical therapy. Resident 165 was observed with her left arm compression sleeve on and without
edema on the left hand.
The facility's policy and procedure titled, admission Assessment and Follow Up: Role of the Nurse, dated
September 2012, indicated, .The purpose of this procedure is to gather information about the resident's
physical, emotional, cognitive, and psychosocial condition upon admission for the purpose of managing the
resident .Contact the Attending Physician to communicate and review the findings of the initial assessment
and any other pertinent information and obtain admission orders that are based on these findings .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 9 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
Based on observation, interview, and record review, the facility failed to ensure pharmacy services were
provided to meet the needs of the residents when:
Residents Affected - Few
1. Two medications for Resident 18 were not administered as ordered by the physician; and
2. One discontinued controlled substance (CS) medication was stored in the medication cart stored with
other active medications available for use.
This failure had the potential for inadequate medication treatment that could cause the resident to
experience pain and constipation, in addition to the potential for ineffective medications to be administered
to the resident.
Findings:
1. On January 9, 2024, at 8:20 a.m., during a medication pass observation with the Licensed Vocational
Nurse (LVN) 2, it was observed, LVN 2 prepared and administered, for Resident 18, her morning
medications that included one potassium chloride (potassium supplement) ER (extended release) 8 MEq
(milliequivalent - unit of measurement) tablet after crushing a total of eight medications.
The eight medications that were administered to the resident by LVN 2 were as follows:
One tablet of amiodarone (medication for irregular heart rhythm) 200 mg (milligram -- unit of measurement);
One tablet of Eliquis (a blood thinner) 5 mg;
One tablet of carvedilol (medication to control blood pressure) 3.125 mg;
One tablet of ezetimibe (medication for high cholesterol) 10 mg;
One tablet of losartan (medication to control blood pressure) 50 mg;
One tablet of metformin (medication to control blood sugar) 500 mg;
One tablet of potassium chloride ER 8 MEq; and
One tablet of rosuvastatin (medication for high cholesterol) 10 mg.
On January 9, 2024, the medical record of Resident 18 was reviewed, and the following was noted:
There was a physician order on December 28, 2023, for docusate sodium (brand name: Colace medication to treat constipation) 100 mg with the direction to give the resident one capsule by mouth one
time a day for bowel management;
There was a physician order on December 21, 2023, for lidocaine external patch 5 % (topical patch for pain
relief) to be applied to the resident's left knee one time a day and be removed per
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 10 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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
schedule; and
Level of Harm - Minimal harm
or potential for actual harm
The electronic medication administration record (eMAR) for January 2024, indicated the morning dose of
docusate sodium 100 mg and lidocaine 5 % patch were documented as administered to the resident;
Residents Affected - Few
The eMAR for January 2024, also indicated the lidocaine topical patch was to be applied at 9 a.m., and
removed at 9 p.m., each day.
On January 9, 2024, at 11 a.m., it was observed Resident 18 still had on her left knee the lidocaine patch
that was applied the day before.
In a concurrent interview, LVN 2 stated he did not administer the lidocaine patch for the resident because
the resident's lidocaine patches ran out, and the resident was going home later that day.
LVN 2 stated he did not administer the resident's morning dose of Colace because the resident was going
home later that day.
LVN 2 stated it was a mistake and he should not have documented as administered the lidocaine patch and
the Colace dose in the resident's medical record.
The facility's policy and procedure titled, Administering Medications, revised, April 2019, was reviewed, and
it indicated:
.Medications are administered in accordance with prescriber orders, including any required time frame .
2. On January 10, 2024, at 1:45 p.m., during an inspection of the medication cart located in [NAME] Hall
with LVN 3, there was a blister pack containing alprazolam (medication to treat anxiety) 0.5 mg tablets for
Resident 15 stored in the CS drawer of the cart with other active controlled substance (CS) medications.
In a concurrent interview, LVN 3 was not able to find in the resident's medical record an active, ongoing
order for alprazolam 0.5 mg.
The resident's medical record was reviewed, and it indicated there was a physician order on November 16,
2023, for alprazolam 0.5 mg with the direction to give the resident one tablet every 23 hours as needed for
anxiety for 14 days as manifested by episodes of verbalization of feeling anxious. There was no additional
order to renew alprazolam 0.5 mg.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 11 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure residents were free from unnecessary
medications for one resident (Resident 214), when two medications in the same therapeutic class were
ordered by the physician and administered to the resident.
Residents Affected - Few
This failure had the potential for the resident to receive excessive dose of medications and unwanted
adverse effects.
Findings:
On January 10, 2024, medical record of Resident 214 was reviewed, and the following was noted:
The resident was admitted to the facility on [DATE], with the diagnoses that included glaucoma (increased
pressure in the eyeball that causes gradual loss of sight);
There was a physician order on December 28, 2023, for Travatan Z (a medication applied directly to eye to
treat glaucoma) 0.004 % eye drop with the direction to instill one drop in both eyes once at bedtime for
glaucoma;
There was a physician order on December 28, 2023, for latanoprost (brand name: Xalatan - a medication
applied directly to eye to treat glaucoma) 0.005 % eye drop with the direction to instill one drop in both eyes
once at bedtime for glaucoma; and
The electronic medication administration record (eMAR) of the resident for January 2024, indicated both
Travatan Z and latanoprost eye drops were administered daily from January 1 to January 10, 2024.
Lexicomp, a nationally recognized drug reference, indicated:
.Travatan Z .Mechanism of Action . A selective FP (prostaglandin receptor F) prostanoid receptor agonist
which lowers intraocular pressure by increasing trabecular meshwork and outflow .
Latanoprost .Mechanism of Action . Latanoprost is a prostaglandin F2-alpha analog believed to reduce
intraocular pressure by increasing the outflow of the aqueous humor .
Avoid combination .Coadministration of latanoprost with additional prostaglandins or prostaglandin analogs
(having similar structure) is not recommended .
On January 11, 2024, at 2:25 p.m., in an interview, the Pharmacist-in-Charge (PIC) of the provider
pharmacy stated the pharmacy identified the therapy duplication with having both Travatan Z and Xalatan
ordered at the same time.
The PIC stated the pharmacy sent a note to indicate and clarify the therapy duplication along with the
delivery of the resident's medications without Travatan Z which was placed on hold.
The PIC agreed there was a therapy duplication.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 12 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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
Level of Harm - Minimal harm
or potential for actual harm
On January 11, 2024, at 2:45 p.m., in an interview, the Director of Nursing (DON) was not aware there was
a request from the pharmacy to clarify the therapy duplication with Travatan Z and Xalatan.
The DON confirmed the resident's eMAR there was documentation both Travatan Z and Xalatan were
administered daily in January 2024.
Residents Affected - Few
The facility's policy and procedure titled, Administering Medications, revised, April 2019, was reviewed and
it indicated:
.If a dosage is believed to be inappropriate or excessive for a resident, or a medication has been identified
as having potential adverse consequences for the resident .the person preparing or administering the
medication will contact the prescriber, the resident's Attending Physician or the facility's Medical Director to
discuss the concerns .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 13 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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
Based on observation, interview, and record review, the facility failed ensure residents were free from
medication error rate greater than 5 % during medication pass observation when:
Residents Affected - Few
- Two medications for Resident 18 were not administered;
- One long-acting extended-release formulation medication was crushed and administered; and
- One long-acting extended-release formulation medication was administered without a full glass of water
being offered.
This failure had the potential for inadequate medication treatment that could cause the resident to
experience pain, constipation, and stomach upset.
The medication error rate was 12.9 percent.
Findings:
On January 9, 2024, at 8:20 a.m., during a medication pass observation with the Licensed Vocational
Nurse (LVN) 2, it was observed, LVN 2 prepared and administered, for Resident 18, her morning
medications that included one potassium chloride (potassium supplement) ER (extended release) 8 MEq
(milliequivalent - unit of measurement) tablet after crushing a total of eight medications.
The eight medications that were administered to the resident by LVN 2 were as follows:
One tablet of amiodarone (medication for irregular heart rhythm) 200 mg (milligram -- unit of measurement);
One tablet of Eliquis (a blood thinner) 5 mg;
One tablet of carvedilol (medication to control blood pressure) 3.125 mg;
One tablet of ezetimibe (medication for high cholesterol) 10 mg;
One tablet of losartan (medication to control blood pressure) 50 mg;
One tablet of metformin (medication to control blood sugar) 500 mg;
One tablet of potassium chloride ER 8 MEq; and
One tablet of rosuvastatin (medication for high cholesterol) 10 mg.
On January 9, 2024, the medical record of Resident 18 was reviewed, and the following was noted:
There was a physician order on November 19, 2023, for potassium chloride ER 8 MEq with the direction to
give the resident one tablet by mouth two times a day for supplement;
There was a physician order on December 28, 2023, for docusate sodium (brand name: Colace (continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 14 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
Level of Harm - Minimal harm
or potential for actual harm
medication to treat constipation) 100 mg (milligram - unit of measurement) with the direction to give the
resident one capsule by mouth one time a day for bowel management;
There was a physician order on December 21, 2023, for lidocaine external patch 5 % (topical patch for pain
relief) to be applied to the resident's left knee one time a day and be removed per schedule; and
Residents Affected - Few
The electronic medication administration record (eMAR) for January 2024 indicated the morning dose of
potassium chloride 8 MEq, docusate sodium 100 mg, and lidocaine 5 % patch were documented as
administered to the resident.
On January 9, 2024, at 11 a.m., in an interview, LVN 26 stated he did not administer lidocaine patch for the
resident because it was not available to administer, and the resident was going home later that day.
LVN 2 stated he did not administer the resident's morning dose of Colace because the resident was going
home later that day.
LVN 2 stated it was a mistake and he should not have documented as administered the lidocaine patch and
the Colace dose in the resident's medical record.
LVN 2 stated the resident preferred the medications to be crushed and they had been crushed and
administered ever since. LVN 2 did not indicate there was a physician order to crush long-acting formulation
of potassium chloride and administer to the resident.
LVN 2 stated he did not offer fluid after administration of crushed medications that included potassium
chloride.
The facility's policy and procedure titled, Administering Medications, revised, April 2019, was reviewed, and
it indicated:
.Medications are administered in accordance with prescriber orders, including any required time frame .
According to the manufacturer's prescribing information for potassium chloride ER tablet:
. Take potassium chloride extended-release tablets with meals and with a glass of water or other liquid. Do
not take on an empty stomach because of its potential for gastric irritation .
Swallow tablets whole without crushing, chewing, or sucking .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 15 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
Level of Harm - Minimal harm
or potential for actual harm
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
Based on observation, interview, and record review, the facility failed to ensure:
Residents Affected - Few
1. One medication stored at bedside for self-administration was properly labeled for Resident 49; and
2. Opened insulin lispro KwikPen (an injectable pen containing insulin, a hormone that regulates blood
sugar) dated with 28-day expiration date was not available for use past the expiration date.
This had the potential for wrong, and ineffective medications to be administered to residents.
Findings:
1. On January 10, 2024, at 2:10 p.m., during inspection of the medication cart located in Red Hall, there
was a manufacturer box for albuterol (medication to treat difficulty breathing) aerosol inhaler, which had a
pharmacy label to indicate it belonged to Resident 49, without the inhaler inside, stored in the bottom
drawer of the cart.
In a concurrent interview, the Licensed Vocational Nurse (LVN) 1 stated the albuterol inhaler was kept at the
resident's bedside inside the resident's room for resident to self-administer the medication.
On January 10, 2024, at 2:35 p.m., it was noted the inhaler was stored in the drawer of the side table next
to the resident's bed. The inhaler was not labeled to indicate it belonged to Resident 49.
In a concurrent interview, the Infection Preventionist (IP) stated the resident's inhaler would be secured in a
locked box. The IP also confirmed there was no label on the resident's albuterol inhaler to indicate it
belonged to the resident.
The facility's policy and procedure titled, Labeling of Medication Containers, revised, April 2019, was
reviewed, and indicated:
.All medications maintained in the facility are properly labeled in accordance with current state and federal
guidelines and regulations .
Labels for individual resident medications include all necessary information, such as:
a. the resident's name;
b. the prescribing physician's names;
c. the name, address, and telephone number of the issuing pharmacy;
d. the name, strength, and quantity of the drug;
e. the prescription number (if applicable);
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 16 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
f. the date that the medication was dispensed;
Level of Harm - Minimal harm
or potential for actual harm
g. appropriate accessory and cautionary statements;
h. the expiration date when applicable; and
Residents Affected - Few
i. directions for use .
2. On January 10, 2024, at 2:10 p.m., during inspection of the medication cart located in Red Hall, there
was a 3-ml insulin lispro (a fast-acting insulin used to prevent high blood sugar) 100 Unit/ml (unit of
measurement) KwikPen for injection with the open date, 12/11/23, that belonged to Resident 49.
The pen also had the following instruction on the label:
Discard 1/8/24. Discard unused portion after 28 days.
On January 11, 2024, at 9:30 a.m., the IP agreed the multidose insulin pen was only good for 28 days after
opening.
The facility's policy and procedure titled, Injectable Medications, revised, October 2018, was reviewed, and
it indicated:
.Multiple use vials (MDV) will expire according to the manufacturer's expiration date printed on the vial
except when special considerations are specified by the manufacturer .All other MDV medications will
expire 28 days after opening per USP Guidelines unless otherwise specified .
According to the manufacturer's prescribing information for insulin lispro 100 units/ml KwikPen:
.Storage and Handling .In-Use (Opened) .28 days Room temperature only (Do not refrigerate) .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 17 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
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 maintain and implement infection prevention
and control practices when the resident's indwelling urinary catheter (catheter used to drain urine from the
bladder into a bag outside the body) drainage bag was touching the floor for one of one resident reviewed
(Resident 164).
Residents Affected - Few
This failure increased the potential to expose Resident 164 for further development of infection and
transmission of communicable diseases.
Findings:
On January 8, 2024, at 12:25 p.m., Resident 164 was observed in a room designated with contact isolation
precautions (steps healthcare facility visitors and staff need to follow before going into a patient's room to
stop germs from spreading by touching the patient or surfaces in the room). The personal protective
equipment (PPE - used to minimize exposure to hazards that cause serious illnesses) cart was observed
outside the room.
During a concurrent observation and interview on January 8, 2024, at 12:28 a.m., with Resident 164 in his
room, Resident 164 was observed lying in bed awake, alert, and able to verbalize his needs.
Resident 164 stated he had infected wounds on his right foot.
A wound vac (device used to remove excess fluid and promote healing of the wounds) was observed on
resident's right side of his foot dressing.
Resident 164 was observed with indwelling urinary catheter attached to a drainage bag containing yellow
urine. The bottom of the indwelling urinary catheter drainage was touching the floor. The drainage bag was
uncovered.
During a concurrent observation and interview on January 8, 2024, at 12:30 p.m., with the Director of
Nursing (DON), in Resident 164's room, the DON stated the resident's indwelling urinary catheter drainage
bag was on the floor. He stated the indwelling urinary drainage bag should not be touching the floor and
should be covered with the dignity bag.
During a concurrent observation and interview on January 8, 2024, at 12:40 p.m., with the Infection
Preventionist (IP), in Resident 164's room, the IP stated the indwelling urinary catheter drainage bag should
not be touching the floor and should be covered with the dignity bag.
On January 8, 2024, Resident 164's record was reviewed. Resident 164 was admitted to the facility on
[DATE], with diagnoses which included End Stage Renal Disease (ESRD - kidney disease), and acute
osteomyelitis (bone infection) of right ankle and foot, and recent right amputation of second and third toes
with Methicillin Resistant Staphylococcus Aureus (MRSA - a serious infection that can lead to sepsis or
death)
During a review of the facility's policy and procedure titled, Catheter Care, Urinary, dated September 2014,
indicated, .The purpose of this procedure is to prevent catheter-associated urinary tract infections .Be sure
the catheter tubing and drainage bag are kept off the floor .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 18 of 19
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
555775
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/11/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshire Rancho Mirage
72-201 Country Club Drive
Rancho Mirage, CA 92270
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0908
Keep all essential equipment working safely.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and record review, the facility failed to maintain the kitchen grill in sanitary
and safe operating condition, when the equipment was covered with blackish materials.
Residents Affected - Few
This failure had the potential to cause cross contamination and unsanitary condition in the kitchen.
Findings:
During the initial tour of the kitchen, conducted on January 8, 2024, beggining at 9:30 a.m., with the
Culinary Director (CD), the kitchen equipment was observed.
During a concurrent observation and inteview on January 8, 2024, at 10:49 a.m., with the CD, the kitchen
grill was observed with blackish materials on the surface and at the sides of the grill. The kitchen grill was
situated next to the kitchen griddle being used by the cook for food preparation.
The CD stated the kitchen grill had not been used for a long time. He further stated the grill should have
been cleaned even if not in use.
During a review of the facility's policy and procedure titled, GRILL - GAS, dated August 31, 2018, indicated,
.SANITATION OF EQUIPMENT .frequency: After each use .Scrape grill to loosen burned-on-particles
.clean grill surface .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555775
If continuation sheet
Page 19 of 19