F 0842
Level of Harm - Potential for
minimal harm
Residents Affected - Some
Safeguard resident-identifiable information and/or maintain medical records on each resident that are in
accordance with accepted professional standards.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview, medical record review, and facility P&P review, the facility failed to ensure the medical record was
accurate and complete for one of five sampled residents (Resident 1).
* Resident 1's informed consent for a bolster pillow was not signed by the provider who had obtained the
informed consent. In additon, there was no physician's order for the use of the bolster pillow. This failure
had the potential for the resident's care needs not being met as their medical information was inaccurate
and incomplete.
Findings:
Review of the facility's P&P titled Informed Consent revised on 3/25/24, showed it is the responsibility of the
healthcare professional who proposes any medical intervention or treatment that requires informed consent
to provide information to the resident/resident representative regarding the resident's condition and
circumstances that are pertinent to a decision to accept or refuse the proposed intervention or treatment.
Medical record review for Resident 1 was initiated on 6/18/25. Resident 1 was admitted to the facility on
[DATE], and was readmitted on [DATE].
Review of Resident 1's H&P examination dated 5/27/25, showed Resident 1 could make needs known but
could not make medical decisions.
Review of Resident 1's care plan dated 6/8/25, showed Resident 1 had an unwitnessed fall from the bed.
The interventions included to have the bilateral bolster pillows to maintain proper body alignment when in
bed.
Review of Resident 1's Physician Document of Informed Consent dated 6/9/25, failed to show the signature
of the provider who had obtained the informed consent.
Review of Resident 1's Medication Review Report for June 2025 failed to show a physician's order for the
use of the bilateral bolster pillow.
On 6/18/25 at 0951 hours, an observation for Resident 1 was conducted. Resident 1's bed had a bilateral
bolster pillow.
On 6/20/25 at 1038 hours, an interview and concurrent medical record review was conducted with LVN
(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:
055984
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
055984
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/20/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Anaheim Healthcare Center, LLC
501 South Beach Blvd.
Anaheim, CA 92804
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 0842
Level of Harm - Potential for
minimal harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
1. LVN 1 confirmed a bolster pillow required a consent from the resident or representative and a physician's
order. LVN 1 verified the bolster pillows did not have an order and the consent was not signed by the
physician.
On 6/20/25 at 1515 hours, an interview and concurrent medical review was conducted with the DON. The
DON verified a bolster pillow required the signature of the provider who obtained the informed consent and
should have a physician's order.
Event ID:
Facility ID:
055984
If continuation sheet
Page 2 of 2