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.
Based on observation, interview, and record review, the facility failed to implement policy and procedure on
safeguarding of all prescribed medications for one of three sampled residents (Resident 3) by failing to
ensure Resident 3's prescribed medication was stored in the medication cart of the nursing station where
Resident 3 was located.
This deficient practice had the potential for non-authorized access to Resident 3's medications.
Findings:
During a record review of Resident 3's admission Record, the admission Record indicated the facility
admitted the resident on 2/21/2024 with diagnoses including type 2 diabetes mellitus (a chronic condition
that affects the way the body processes blood sugar [glucose]), essential hypertension (an abnormally high
blood pressure that was not a result of a medical condition), and depression (a constant feeling of sadness
and loss of interest, which stops the individual from doing normal activities).
During a record review of Resident 3's Minimum Data Set (MDS - a resident assessment tool), dated
11/27/2024, the MDS indicated the resident's cognitive (refers to conscious mental activities including
thinking, reasoning, understanding, learning, and remembering) skills were intact.
During a concurrent observation and interview on 1/28/2025 at 9:20 a.m. with Licensed Vocational Nurse 1
(LVN 1), LVN 1 opened the first top drawer at nurse station 400 and observed a medication container
labeled Airshield (a medication brand name) dietary supplement with Resident 3's name and room number.
LVN 1 stated Resident 3 was a current resident in the facility. LVN 1 stated medications should be placed
inside the locked medication cart or inside the locked medication room.
During a follow up interview on 1/28/2025 at 10:35 a.m. and a concurrent record review of Resident 3's
medical records, reviewed with LVN 1, LVN 1 stated Resident 3's Physician Order did not indicate an order
for Airshield dietary supplement. LVN 1 stated medications that were discontinued should be disposed
inside the locked medication room. LVN 1 stated residents' medications stored in an unlocked nurse station
drawers had the potential for another resident to ingest the medication and result I adverse effects
(unwanted and undesirable effects of a medication).
During an interview on 1/28/2025 at 2:40 p.m. with the Director of Nursing (DON), the DON stated Resident
3's discontinued medication should be inside the locked medication room. The DON stated other residents
had the potential to have access to Resident 3's medication and cause the other resident adverse effects.
The DON stated the facility failed to follow the policy and procedures on
(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 3
Event ID:
555583
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
555583
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/28/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
MacLay Healthcare Center
12831 MacLay Street
Sylmar, CA 91342
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
medication storage.
Level of Harm - Minimal harm
or potential for actual harm
During a review of the facility's policy and procedure (PnP) titled, Storage of Medications, last reviewed on
4/2024, the PnP indicated the facility stores all drugs and biologicals in a safe, secure, and orderly manner.
The PnP indicated discontinued, outdated, or deteriorated drugs or biologicals are returned to the
dispensing pharmacy or destroyed. The PnP indicated compartments containing drugs and biologicals are
locked when not in use. The PnP indicated unlocked medication carts are not left unattended.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555583
If continuation sheet
Page 2 of 3
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
555583
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/28/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
MacLay Healthcare Center
12831 MacLay Street
Sylmar, CA 91342
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 0760
Ensure that residents are free from significant medication errors.
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 one of three sampled residents
(Resident 1) was free from significant medication errors by failing to ensure the physician orders were
followed. Resident 1's medication dose was not clarified with the attending physician.
Residents Affected - Few
This deficient practice placed Resident 1 at risk for medication administration error that had the potential to
result in difficulty in breathing.
Findings:
During a record review of Resident 1's admission Record, the admission Record indicated the facility
admitted the resident on 9/23/2021 and readmitted on [DATE] with diagnoses including metabolic
encephalopathy (an alteration in consciousness due to brain dysfunction), chronic obstructive pulmonary
disease (COPD - a lung disease characterized by long term poor airflow), and muscle weakness.
During a record review of Resident 1's Minimum Data Set (MDS - a resident assessment tool), dated
1/20/2025, the MDS indicated the resident's cognitive (refers to conscious mental activities including
thinking, reasoning, understanding, learning, and remembering) skills were intact.
During an observation and concurrent interview on 1/28/2025 at 9:24 a.m. with Licensed Vocational Nurse
1 (LVN 1), observed Resident 1's medication box indicated Atrovent (a medication used to relax muscles in
the airway and increases air flow to the lungs) 17 micrograms (mcg - unit of measurement) inhaler. LVN 1
stated Resident 1's medication label indicated one puff by mouth every 24 hours as needed for shortness
of breath, wheezing, or COPD.
During an interview on 1/28/2025 at 9:26 a.m. and a concurrent record review of Resident 1's Physician
Orders, reviewed with LVN 1 the Physician Orders, dated 1/25/2025, indicated Atrovent HFA aerosol
solution (a substance released in very fine mist) 17 mcg four puffs inhale orally every 24 hours as needed
for shortness of breath, wheezing, or COPD. LVN 1 stated Resident 1's Medication Administration Record
(MAR) indicated the resident did not receive any dose of Atrovent since the resident was readmitted from
General Acute Care Hospital 1 (GACH 1). LVN 1 stated Resident 1's Nursing Note, dated 1/25/2025 at 3:23
p.m., indicated Registered Nurse 2 (RN 2) received a pharmacy note that indicated the resident's Atrovent
HFA four puffs exceed the maximum single dose of 2 puffs. LVN 1 stated there was no physician order for
Resident 1's Atrovent HFA one puff by mouth every 24 hours. LVN 1 stated the Resident 1 had the potential
to receive the wrong medication dose.
During an interview on 1/28/2025 at 2:40 p.m. with the Director of Nursing (DON), the DON stated RN 2 did
not verify Resident 1's medication dosage and frequency with the attending physician. The DON stated
Resident 1 had the potential to receive a wrong dose of the medication. The DON stated the facility failed to
ensure medications were clarified with the attending physician.
During a record review of the facility's policy and procedure (PnP) titled, Medication Administration, last
reviewed on 4/2024, the PnP indicated any dose or order that appears inappropriate considering the
resident's age, condition, or diagnosis is verified with the attending physician before processing. The PnP
indicated the facility pharmacy will not process a medication order if it is unclear or confusing, until the
clarification was made.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555583
If continuation sheet
Page 3 of 3