F 0554
Allow residents to self-administer drugs if determined clinically appropriate.
Level of Harm - Potential for
minimal harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and the facility P&P review, the facility failed to ensure one of four sampled residents
(Resident 3) was assessed to determine if it was safe for the resident to self-administer the medications. *
Resident 3 was observed with a medication cup filled with multiple medications at the bedside table.
Resident 3 had no assessment, physician's order, and/or care plan problem addressing the
self-administration of the medications. This failure had the potential for Resident 3 to administer
medications inaccurately.Findings: Review of the facility's P&P titled Self-Administration of Medications
(undated) showed the following:a. Residents will be informed that they have a right to self-administer drugs
upon admission;b. if a resident requests to self-administer drugs the IDT will determine if the practice is
safe before the resident may exercise this right;c. the IDT will determine who is responsible for the storage
of the drugs and documentation of the administration of drugs, as well as the location of Drug
Administration;d. these determinations need to be included in the residence care plan; e. the physicians
order for such drugs will be clarified to include may keep at bedside; andf. residents who self-administer
drugs will be periodically reevaluated based on any changes in the resident's status. Medical record review
for Resident 3 was initiated on 7/24/25. Resident 3 was admitted to the facility on [DATE]. On 7/24/25 at
1108 hours, a concurrent observation and interview was conducted with Resident 3. A medication cup filled
with multiple medications were present at the resident's bedside. When Resident 3 was asked if the
medications inside the medication cup belong to him, Resident 3 stated Yes, then proceeded to
self-administer the medications without the licensed nurse present. Review of Resident 3's Order Summary
Report dated 7/24/25, failed to show a physician's order to self-administer the medications. Further review
of Resident 3's medical record failed to show Resident 3 was assessed for the self-administration of the
medications. Review of Resident 3's plan of care failed to show a care plan problem to address Resident
3's ability to self-administer the medications. On 7/24/25 at 1114 hours, an interview was conducted with
LVN 1. LVN 1 was informed of the above findings. LVN 1 verified Resident 3 was not supposed to have the
medications unattended at the bedside. LVN 1 stated the facility's process for the residents to
self-administer the medications require an assessment from the physician to indicate the resident could
self-administer the medications. On 7/24/25 at 1454 hours, a follow up interview was conducted with LVN 1.
LVN 1 verified the medications inside the medication cup were Resident 3's scheduled at 0900 hours
medications. When asked what medications were inside the medication cup, LVN 1 stated the following
medications: folic acid (supplement), amlodipine (blood pressure medication), carvedilol (blood pressure
medication), apixaban (blood thinner medication), aspirin (blood thinner), vitamin D (supplement), and
lisinopril (blood pressure medication). On 7/25/25 at 1548 hours, an interview and concurrent medical
record review was conducted with the DON. The DON stated the following medications were documented
as administered to the resident on 7/24/25 at 0900 hours: amlodipine, aspirin, cyanocobalamin (vitamin b12
supplement),
Residents Affected - Some
(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 2
Event ID:
555249
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
555249
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sea Cliff Healthcare Center
18811 Florida St
Huntington Beach, CA 92648
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
Level of Harm - Potential for
minimal harm
folic acid, Lasix (diuretic), lisinopril, thiamin (supplement), and apixaban. The DON verified Resident 3 had
no assessment, physician's order, and/or a care plan problem addressing the self-administration of the
medications. On 7/25/25 at 1617 hours, an interview was conducted with the Administrator and DON. The
Administrator and the DON were informed and acknowledged the above findings.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555249
If continuation sheet
Page 2 of 2