F 0657
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop the complete care plan within 7 days of the comprehensive assessment; and prepared, reviewed,
and revised by a team of health professionals.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure a care plan was initiated and/or
developed to address the diagnoses of epistaxis (bleeding from the nose) for one of one residents reviewed
for quality of care (Resident 1).This failure had the potential for Resident 1 to not be monitored for epistaxis
complications and delayed treatment, increasing the risk of further harm. Findings:On November 25, 2025,
at 8:00 a.m. an unannounced visit was conducted at the facility to investigate a facility reported incident.On
November 25, 2025, at 8:00 a.m., an observation with a concurrent interview was conducted with Resident
1. Resident 1 was observed in bed, alert and interviewable. Red stains resembling blood were observed on
Resident 1's gown, specifically in the chest area. Similar stains were also noted on a washcloth located
beside Resident 1. Resident 1 stated she experienced nose bleeds often. On November 25,2025, at 8:
15a.m, an interview was conducted with Licensed Vocational Nurse (LVN) 1. LVN 1 stated Resident 1 had
episodes of nose bleeding since she started working at the facility about a month ago. LVN 1 stated
Resident 1's episodes of nose bleeds have been referred to her primary physician.On November 25, 2025,
Resident 1's record was reviewed. Resident 1 was readmitted to the facility on [DATE] with diagnoses
including Right Distal Femur Fracture (broken leg).The Nurse Practitioner (NP) progress notes, dated
November 4, 9, 12, 16, 19, and 24, 2025, indicated Resident 1 had epistaxis. There was no documented
evidence that a care plan was developed to address Resident 1's epistaxis during these dates.On
November 25,2025 at 9:30 a.m., an interview with a concurrent record review was conducted with the
Director of Nursing (DON). The DON stated:- Resident 1 had history of nose bleeding prior to her
hospitalization on November 4, 2025;-Resident 1 had epistaxis as noted by the NP on November 4, 9, 12,
16, 19, and 24, 2025;-Resident 1 was being monitored for the side effects of anticoagulant (blood-thinning
medicine that helps prevent clots) and antiplatelet (medicine that prevents blood cells from sticking together
to make clots) medication, such as nosebleeds. The electronic Medication Administration Record (eMAR)
dated November 1 to 30, 2025, showed no episodes of nose bleeds from November 9 to 25, 2025.- There
was no documentation the licensed nurses identified and referred to the physician Resident 1's episodes of
epistaxis from November 9 to 24, 2025;- There was no care plan developed or initiated to address Resident
1's epistaxis since she was re-admitted from the acute hospital on November 4, 2025; and- A care plan
should have been initiated on November 4, 2025, to monitor Resident 1's need for interventions to address
epistaxis. In addition, a care plan was needed to communicate the plan of care to address Resident 1's
epistaxis. The facility's policy and procedure titled, Care Plans, Comprehensive Person-Centered, dated
and revised in December 2016, indicated, .Care plans shall incorporate goals and objectives that lead to
the resident's highest obtainable level of independence .Goals and objectives are reviewed and/or revised
when there has been a significant change in the resident's condition .When the resident has been
readmitted to the facility from a
(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:
555711
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
555711
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Community Care on Palm
4768 Palm Avenue
Riverside, CA 92501
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0657
hospital/rehabilitation stay; and at least quarterly .
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:
555711
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
555711
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Community Care on Palm
4768 Palm Avenue
Riverside, CA 92501
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure two of two residents reviewed for
breathing treatment therapy (Residents 4 and 2), were monitored during and after nebulizer treatments
(breathing treatments that turn liquid medicine into a mist).This failure placed the residents at risk for
delayed treatment related to possible complications of the nebulizing treatment such as rapid heart rate,
restlessness, chest pain and/or difficulty breathing.Findings:1.On November 25, 2025, at 8:30 a.m., and
observation was conducted with Resident 4. Resident was in bed, alert, and non-verbal. A nebulizer mask
(mask used to breathe in medicated mist) was observed connected over her nose and mouth. The
medication chamber (small cup that holds the liquid medicine) was observed empty. There was no licensed
nurse observed beside Resident 4.On November 25, 2025, at 8:45 a.m., an interview was conducted with
Licensed Vocational Nurse (LVN) 1. LVN 1 stated she should have stayed in the room with Resident 4
during the breathing treatment per facility policy. On November 25, 2025, at 9:10 a.m., an observation with
a concurrent interview was conducted with LVN 1. She stated she was the licensed nurse assigned to
Resident 4 and she administered the breathing treatment (misted medication session) at 8:00 a.m. LVN 1
stated each breathing treatment last approximately 15-20 minutes. LVN 1 stated she had left the room
because another resident had called for assistance. LVN 1 stated the correct procedure was to remain with
the resident during the breathing treatment to observe for difficulty breathing (trouble catching their breath).
LVN 1 stated the possible outcome of leaving the mask on the resident after the medication was gone was
that the resident may become anxious, have trouble breathing, or refuse the next treatment. On November
25, 2025, at 9:10 a.m. LVN 1 was observed removing the nebulizing mask off Resident 4.On November 25,
2025, Resident 4's record was reviewed. Resident 4 was admitted to the facility on [DATE], with diagnosis
including hypoxia (low oxygen level in the blood).The physician's order dated December 4, 2024, indicated
to administer .Albuterol Inhalation Solution 0.5-2.5 (3) MG(milligram-unit of measurement)/3(ML)
(millimeter-unit of measurement) (Ipratropium-Albuterol) 1 Vial (nebulizer medication treatment/misted
medication) . To be given three times a day for shortness of breath. The electronic Medication
Administration Record (eMAR) dated November 25, 2025, indicated LVN 1 administered the medication
Albuterol to Resident 4 at 8 a.m.On November 25, 2025 at 9:30 a.m., an interview was conducted with the
Director of Nursing (DON). The DON stated the licensed nurse was expected to remain with the resident
during breathing treatment and remove the nebulizer face mask when the treatment was completed. 2. On
November 25, 2025, at 8:54 a.m., an observation was conducted with Resident 2. Resident 2 was observed
in bed, alert and oriented. Resident 2 had a nebulizer face mask in place with no medication solution
remaining in the medication chamber. Resident 2 was observed with no licensed nurse present at bedside.
On November 25, 2025, at 9:10 a.m., an interview was conducted with LVN 2. LVN 2 stated the correct way
to administer a nebulizer treatment (breathing-mist medication) is to observe the resident for any difficulty
breathing (trouble catching their breath) and remain with the resident during medication administration. LVN
2 stated it was not acceptable to leave the mask on Resident 2 for an hour because there is no medication
solution left. LVN 2 stated she gave the breathing treatment medication, left the resident, and did not turn
off the machine until 9:10 a.m. LVN 2 stated the possible outcome of leaving the mask on for that length of
time is the resident might become anxious and refuse the next breathing treatment. LVN 2 stated she left
the room because she was called out to assist another resident. LVN 2 stated that Resident 2 had the face
mask on for an hour. LVN 2 stated each breathing treatment (mist medication session) lasts approximately
15 minutes. On November 25, 2025, Resident 2's record was reviewed. Resident 2 was
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555711
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
555711
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Community Care on Palm
4768 Palm Avenue
Riverside, CA 92501
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
admitted to the facility on [DATE], with diagnosis including Chronic Respiratory Failure with Hypoxia (low
oxygen in the blood)A physician order dated April 4,2025, indicated to administer, .Budenoside Inhalation
suspension (breathing treatment medication) 0.5 MG (milligrams- unit of measurement)/2ML (milliliters unit of measurement) 1 mg inhale two times a day related to for Chronic Obstructive Pulmonary Disease
with Exacerbation (a long-term lung disease that makes it hard to breath, with a recent flare-up/worsening
episode) . The electronic Medication Administration Record (eMAR) dated November 25, 2025 indicated
LVN 2 administered the medication Budenoside at 8:00 a.m. On November 25,2025 at 9:30 a.m., an
interview was conducted with the Director of Nursing (DON) The DON stated the licensed nurse should
have removed Resident 2's nebulizer face mask once the medication was completed and monitored the
resident during and after the treatment for any signs of difficulty breathing, anxiety, or distress. The DON
stated this practice was required to ensure resident safety during breathing treatments.The facility's policy
and procedure titled, Administering Medications Through a Small Volume Nebulizer, dated October 2010
was reviewed. The policy indicated, .The purpose of this procedure is to safely and aseptically (free from
contamination) administer aerosolized particles of medication into the resident's airway . General guidelines
are to follow the medication administration guidelines in the policy entitled Administering Medications
.Steps in the Procedure .Assemble nebulizer equipment and attach to the source of gas per manufacture's
instructions .Turn off the nebulizer and check the outflow port for visible mist .Instruct the resident to take a
deep breath, pause briefly and then exhale normally .Encourage the resident to repeat the above breathing
pattern until the medication is completely nebulized, or until the designated time of treatment has been
reached .Remain with the resident for the treatment .Monitor for medication side effects, including rapid
pulse, restlessness and nervousness throughout the treatment .Encourage the resident to cough and
expectorate as needed .Administer therapy until it is gone .When treatment is complete, turn off nebulizer
and disconnect T-piece, mouthpiece and medication cup .Obtain post-treatment pulse, respiratory rate and
lung sounds .
Event ID:
Facility ID:
555711
If continuation sheet
Page 4 of 4