F 0580
Level of Harm - Potential for
minimal harm
Residents Affected - Some
Immediately tell the resident, the resident's doctor, and a family member of situations (injury/decline/room,
etc.) that affect the resident.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and medical record review, the facility failed to notify the resident's representative when there was
a change of the POA for one of four sampled residents (Resident 1).
* Resident 1's legal representative was changed from Family Member 1 to Family Member 2 without
informing Family Member 1. This failure resulted in Family Member 1 being unaware of the change, which
had the potential to negatively impact the resident's well-being.
Findings:
On 1/2/24 at 0816 hours, a telephone interview was conducted with Family Member 1. Family Member 1
stated she was the POA for Resident 1; however, the facility changed the POA to Family Member 2 without
informing her.
Medical record review for Resident 1 was initiated on 1/2/24. Resident 1 was admitted to the facility on
[DATE], and readmitted on [DATE].
Review of Resident 1's History and Physical Form dated 2/28/23, showed Resident 1 did not have the
capacity to understand and make decisions.
Review of Resident 1's History and Physical Form dated 7/13/23, showed Resident 1 did have the capacity
to understand and make decisions.
Review of Resident 1's Progress Note dated 7/20/23 at 1217 hours, showed Resident 1 was assisted to
complete a new Advance Health Care Directive, designating Family Member 2 as his Power of Attorney.
There was no documentation showing Family Member 1 was made aware.
Review of Resident 1's Progress Note dated 9/26/23 at 1521 hours, showed Family Member 2 was left a
voicemail regarding the change in Power of Attorney.
On 1/2/24 at 1147 hours, an interview and concurrent medical record review was conducted with the SSA.
The SSA verified Resident 1 changed his POA from Family Member 1 to Family Member 2 on 7/19/23, after
his physician deemed him capable of understanding and making medical decisions. The SSA stated she
called Family Member 1 and left a voicemail to inform her, but forgot to document the call. The SSA was
unable to show any documentation Family Member 1 was made aware of the change of POA prior to
9/26/23.
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:
555667
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
555667
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/05/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Garden Park Care Center
12681 Haster Street
Garden Grove, CA 92840
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 0690
Level of Harm - Potential for
minimal harm
Residents Affected - Some
Provide appropriate care for residents who are continent or incontinent of bowel/bladder, appropriate
catheter care, and appropriate care to prevent urinary tract infections.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and medical record review, the facility failed to ensure a physician's order was in
place prior to the use of an indwelling urinary drainage catheter for one of four sampled residents (Resident
3). This failure put Resident 3 at risk of complications and not having their care needs met.
Findings:
On 1/2/24 at 1354 hours, an observation was conducted at Resident 3's bedside. Resident 3 was observed
in bed with an indwelling urinary drainage catheter in place.
Medical record review for Resident 3 was initiated on 1/2/24. Resident 3 was admitted to the facility on
[DATE], and readmitted on [DATE].
Review of Resident 3's Order Summary Report failed to show a physician's order for the use of an
indwelling urinary drainage catheter.
On 1/5/24 at 1137 hours, an observation, interview, and concurrent medical record review was conducted
with LVN 1. Resident 3 was again observed in bed with an indwelling urinary drainage catheter in place.
LVN 1 was asked about Resident 3's indwelling urinary drainage catheter. LVN 1 stated Resident 3 had the
indwelling urinary drainage catheter since his readmission. LVN 1 was asked to show the physician's order
for the use of the indwelling urinary drainage catheter. LVN 1 reviewed the medical record and was unable
to find a physician's order. LVN 1 stated there should be a physician's order prior to the use of an indwelling
urinary drainage catheter.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555667
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
555667
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/05/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Garden Park Care Center
12681 Haster Street
Garden Grove, CA 92840
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
Residents Affected - Few
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and medical record review, the facility failed to administer the medications as ordered by the
physician for one of four sampled residents (Resident 3).
* Resident 3 had a physician's order for insulin glargine (a medication used to treat diabetes) to be given at
bedtime, with parameters to hold if the blood sugar levels were less than 120 mg/dl. There was no
documented evidence the blood sugar level was checked to determine whether to administer or hold the
insulin as ordered. This failure put Resident 3 at risk of complications.
Findings:
Medical record review for Resident 3 was initiated on 1/2/24. Resident 3 was admitted to the facility on
[DATE], and readmitted on [DATE].
Review of Resident 3's Order Summary Report showed an order dated 12/26/23, for insulin glargine 100
unit/ml 6 units subcutaneously (under the skin) at bedtime for DM and to hold if the blood sugar levels were
less than 120 mg/dl.
Review of Resident 3's Medication Administration Record showed Resident 3 received insulin glargine as
ordered from 1/1 - 1/4/24; however, there was no documented evidence of blood sugar levels.
On 1/5/24 at 1137 hours, an interview and concurrent medical record review was conducted with LVN 1.
LVN 1 verified Resident 3 had an order for insulin glargine at bedtime with the instructions to hold if the
blood sugar levels were less than 120 mg/dl. LVN 1 was asked to show documentation the blood sugar
levels were checked prior to the insulin administration and was unable to do so.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555667
If continuation sheet
Page 3 of 3