F 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Honor the resident's right to request, refuse, and/or discontinue treatment, to participate in or refuse to
participate in experimental research, and to formulate an advance directive.
**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 maintain a copy of one of 19
final sampled residents' (Resident 12) advance directive in the medical record to ensure it was readily
available to the facility staff. This had the potential for the resident's decisions regarding their healthcare
and treatment options not being honored.
Findings:
Review of the facility's P&P titled Advance Directives revised 2/2022 showed if a resident has executed an
advance directive, the facility must obtain a copy from the resident or legal representative. The facility's copy
of the advance directive must be filed in the resident's clinical record.
Medical record review for Resident 12 was initiated on 11/15/22. Resident 12 was admitted to the facility on
[DATE] and readmitted on [DATE].
Review of the Physician Orders for Life-Sustaining Treatment (POLST) dated 6/9/22, showed Resident 12
had formulated an advance directive.
Review of Resident 12's Social Service Assessment admission and re-admission dated 6/2/22, showed
Resident 12's family member provided a copy of the resident's advance directive to the facility.
However, review of Resident 12's medical record failed to show a copy of the resident's advance directive.
On 11/16/22 at 1344 hours, an interview and concurrent medical record review was conducted with RN 1.
RN 1 was informed and verified the above finding. RN 1 stated Resident 12 had formulated an advance
directive; however, a copy of the advance directive was not readily available in the resident's medical
record.
On 11/16/22 at 1404 hours, an interview and concurrent medical record review was conducted with the
Medical Records Director. After searching the overflow medical records two times, the Medical Records
Director stated she found the copy of Resident 12's advance directive. The Medical Records Director
verified a copy of the advance directive must be included in the medical record so it was readily available to
any facility staff.
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 8
Event ID:
055575
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
055575
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pacific Haven Subacute and Healthcare Center
12072 Trask Ave.
Garden Grove, CA 92843
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 0692
Provide enough food/fluids to maintain a resident's health.
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 medical record review, the facility failed to ensure one of 19 final sampled
residents (Resident 14) was administered the prescribed enteral formula (liquid nourishment administered
through a GT) as ordered by the physician. This failure posed the risk for Resident 14 to have unplanned
weight loss.
Residents Affected - Few
Findings:
During the tour of the facility on 11/17/22 at 0758 hours, Resident 14 was observed lying in bed with a
continuous feeding pump infusing at 70 ml per hour from a 1500 ml bottle of Jevity (fiber-fortified
tube-feeding formula) 1.5 Cal
Medical record review for Resident 14 was initiated on 11/17/22. Resident 14 was admitted to the facility on
[DATE], and readmitted on [DATE].
Review of the physician's order dated 11/14/22, showed to administer Jevity 1.5 Cal at 80 ml per hour via
GT for 20 hours to provide 1600 ml/2400 calories.
On 11/17/22 at 0813 hours, an observation and concurrent interview was conducted with the ADON and
DON. The ADON and DON verified the rate of the enteral formula administered to Resident 14 was
incorrect. The ADON and DON stated Resident 14 should be administered Jevity 1.5 Cal at 80 ml per hour
as per the physician's order. The DON then adjusted the rate of the feeding pump to 80 ml per hour.
On 11/17/22 at 1523 hours, a follow-up interview was conducted with the DON. When asked what was the
possible harm of not receiving the GT feeding as prescribed by the physician, the DON replied it could
result in Resident 14's dehydration and weight loss.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055575
If continuation sheet
Page 2 of 8
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
055575
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pacific Haven Subacute and Healthcare Center
12072 Trask Ave.
Garden Grove, CA 92843
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 facility P&P review, the facility failed to provide the respiratory care to meet the
needs for one of 19 final sampled residents (Resident 64). The facility failed to ensure the mechanical
ventilator low pressure alarm for Resident 64 was set within the safe parameters as per the facility's P&P.
This posed the risk for delayed care and interventions if the resident's ventilator alarm was not trigerred
when it should have, to alert the staff the resident was in distress or disconnected from their ventilator.
Residents Affected - Few
Findings:
Review of the facility's P&P titled Mechanical Ventilation (undated) showed to set the ventilator low pressure
alarm 5 to 10 cmH2O below the PIP.
According to the Clinical Application of Mechanical Ventilation 2014, Fourth Edition, the low-pressure alarm
is triggered if the PIP is less than the alarm setting. Conditions that may trigger the low-pressure alarm may
include circuit disconnection, exhalation valve driveline disconnection, endotracheal tube cuff leak, and a
loose circuit connection.
On 11/15/22 at 0848 hours, Resident 64 was observed in bed with a tracheostomy tube in place and
connected to a mechanical ventilator. The observed PIP on the ventilator was 40 and the low pressure
alarm was observed set at 15.
Medical record review for Resident 64 was initiated on 11/15/22. Resident 64 was admitted to the facility on
[DATE] and readmitted on [DATE].
On 11/15/22 at 1408 hours and 11/16/22 at 0808 and 1416 hours, Resident 64 PIP range was 41 to 46 and
the low pressure alarm was set at 15.
On 11/16/22 at 1421 hours, an observation of Resident 64's ventilator settings was conducted with RT 1.
RT 1 verified how to check the ventilator settings. RT 1 verified Resident 64's average observed PIP on the
ventilator was in the 40s and the low pressure alarm should be set 10 cmH2O below the PIP. RT 1 verified
Resident 64's low pressure alarm was set at 15 instead of 30 based on the resident's average observed
PIP. RT 1 stated the low pressure alarm was important because it would alert the staff if the resident was
disconnected from the ventilator.
On 11/16/22 at 1445 hours, an interview was conducted with RT 2. RT 2 verified the low pressure alarm
should be set 5 to 10 cmH2O below the resident's observed PIP. Cross reference to F842.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055575
If continuation sheet
Page 3 of 8
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
055575
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pacific Haven Subacute and Healthcare Center
12072 Trask Ave.
Garden Grove, CA 92843
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 0759
Ensure medication error rates are not 5 percent or greater.
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 clinical record review, the facility failed to ensure the medication error rate was
below 5%. The facility's medication error rate was at 6.67% when the metoprolol (antihypertensive)
medication for one of 19 final sampled residents (Resident 89) and one of one nonsampled resident
(Resident 29) were not administered with food as per the manufacturer's specifications. This failure created
the risk for complications and ineffective therapeutic effects of the medications.
Residents Affected - Few
Findings:
According to Lexicomp.com (a professional resource or a nationally recognized drug information site for
healthcare professionals), metoprolol tartrate medication should be taken with or immediately after food
intake.
a. During the medication administration observation on 11/17/22 at 0840 hours, the GT was clamped during
the medication pass. LVN 1 administered metoprolol 10 mg to Resident 89 via GT. LVN 1 was asked when
Resident 89 finished her breakfast. LVN 1 stated the GT feeding was turned off at around 0730 hours. LVN
1 further stated Resident 89 was in the RNA program eating at dining room and finished her breakfast meal
at around 0800 hours.
On 11/17/22 at 1015 hours, an interview was conducted with RNA 1. RNA 1 was asked when Resident 89
finished her breakfast meal. RNA 1 replied at around 0800 hours.
Review of Resident 89's medical record was initiated on 11/17/22. Resident 89 was admitted to the facility
on [DATE].
Review of the Order Summary report dated 10/30/22, showed to administer metoprolol tartrate 25 mg one
tablet via the GT every 12 hours for high blood pressure and to hold if the systolic blood pressure less than
110 mmHg or heart rate less than 60 bpm.
On 11/17/22 at 1205 hours, an interview was conducted with the Pharmacy Consultant. The Pharmacy
Consultant was asked regarding the administration instructions on the bubble pack of metoprolol to
administer with or immediately after food intake. The Pharmacy Consultant stated the reason for
administering with food was to prevent stomach upset and should be administered within 15 minutes after
eating the food or with the food.
b. On 11/17/22 at 0915 hours, Resident 29 pressed the call light to ask CNA 2 for snacks for her and her
roommate. However, CNA 2 did not bring a snack for Resident 29 prior to the medication administration.
During a medication administration observation on 11/17/22 at 0940 hours, LVN 1 administered the
metoprolol medication to Resident 29 with cranberry juice. However, LVN 1 did not administer the
medication with food as per the manufacturer's specification.
On 11/17/22 at 1030 hours, CNA 1 was asked when did Resident 29 finished her breakfast meal. CNA 1
stated Resident 29 had her breakfast meal at around 0800 hours.
Review of Resident 29's medical record was initiated on 11/17/22. Resident 29 was admitted to the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055575
If continuation sheet
Page 4 of 8
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
055575
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pacific Haven Subacute and Healthcare Center
12072 Trask Ave.
Garden Grove, CA 92843
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 0759
facility on [DATE] and readmitted to the facility on [DATE].
Level of Harm - Minimal harm
or potential for actual harm
Review of the Order Summary report dated 10/30/22, showed to administer metoprolol tartrate 25 mg one
tablet orally two times a day for hypertension (high blood pressure) and hold the medication if the systolic
blood pressure was less than 110 mmHg or the heart rate was less than 60 bpm.
Residents Affected - Few
On 11/17/22 at 1226 hours, an interview was conducted with LVN 1. LVN 1 was asked if she was aware the
metoprolol medication should be administered with food or immediately after food intake. LVN 1 stated she
was not aware of it. LVN 1 acknowledged the metoprolol medication was administered to Residents 89 and
29 approximately more than 40 minutes after both residents had eaten their breakfast meals. LVN 1 verified
the findings.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055575
If continuation sheet
Page 5 of 8
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
055575
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pacific Haven Subacute and Healthcare Center
12072 Trask Ave.
Garden Grove, CA 92843
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 0812
Level of Harm - Minimal harm
or potential for actual harm
Procure food from sources approved or considered satisfactory and store, prepare, distribute and serve
food in accordance with professional standards.
Based on observation, interview, and facility document review, the facility failed to ensure the food safety
and sanitation requirements were met in the kitchen as evidenced by the following:
Residents Affected - Some
* The facility failed to ensure the can openers were in sanitary condition and free of food particles; the
kitchen utensils had a smooth cleanable surface and were not worn out; the kitchen equipment was air
dried and free of food particles; and the kitchen utensils were clean and free of food particles.
* The facility failed to ensure the sanitary condition of the hood over the stove was maintained.
These failures had the potential to cause foodborne illnesses in a medically vulnerable resident population
who consumed food prepared in the kitchen.
Findings:
Review of the Form CMS-672 titled Resident Census and Conditions of Residents completed by the facility
dated 11/15/22, showed 49 out of 95 residents residing in the facility received food prepared in the kitchen.
1. According to the USDA Food Code 2017, Section 4-101.11, Multiuse, Characteristics, materials that are
used in the construction of utensils and food contact surfaces of equipment may not allow the migration of
deleterious (harmful) substances or impart colors, odors, or tastes to food and under normal use conditions
shall be durable, corrosion-resistant, nonabsorbent, finished to have a smooth, easily cleanable surface,
and resistant to pitting, chipping, crazing, scratching, scoring, distortion, and decomposition.
According to the USDA Food Code 2017, Section 4-901.11, Equipment and Utensils, Air-Drying Required,
items must be allowed to drain and to air-dry before being stacked or stored. Stacking wet items prevents
them from drying and may allow an environment where microorganism can begin to grow.
According to the FDA Food Code, 2017 4-601.11, it is the standard of practice to ensure non-food contact
surfaces of equipment shall be kept free of an accumulation of dust, dirt, food residue, and other debris.
According to the FDA Food Code Annex 4-602.13, the presence of food debris or dirt on nonfood contact
surfaces may provide a suitable environment for the growth of microorganisms which employees may
inadvertently transfer to food. If these areas are not kept clean, they may also provide harborage for
insects, rodents, and other pests.
During the initial tour of the facility's kitchen on 11/15/22 at 0808 hours, a concurrent observation and
interview was conducted with the Dietary Aide 1. The following was identified:
- A counter mounted can opener and a portable can opener were observed with brownish discoloration
(metal part) and dry food residue. Dietary Aide 1 verified the findings.
- A flipper spatula was observed to be chipped and worn off. The Dietary Aide 1 verified the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055575
If continuation sheet
Page 6 of 8
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
055575
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pacific Haven Subacute and Healthcare Center
12072 Trask Ave.
Garden Grove, CA 92843
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 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
finding and stated it was not safe to use because residual particles from the spatulas could be mixed with
food.
- A white blender was observed stored on the counter shelves. The blender's lid was still wet inside, and
there was visible white food residue on the blender. The Dietary Aide 1 verified the finding and stated the
equipment should have been stored dry.
- A knife with a black handle was observed with dry, crusted food residue. The Dietary Aide 1 verified the
finding and stated the knife should have been washed and cleaned properly to prevent food contamination.
On 11/15/22 at 0855 hours, a concurrent observation and interview was conducted with the Food and
Nutrition Services Director. The Food and Nutrition Services Director verified the above findings and stated
everything should be washed and cleaned for safety, cross contamination, the possibility for food borne
pathogen illnesses and infection control.
2. Review of the facility's P&P titled Kitchen Safety dated 2018 showed grease fires are common and
dangerous. Vents in range hoods should be cleaned regularly, at least monthly, depending on extent of use.
Know the locations of the nearest fire extinguisher and how to use them. Sides of floors around ranges
should be cleaned daily. If the fire is on the stove, use the K (silver) fire extinguisher or pull the ansel
system.
On 11/17/22 at 1235 hours, an observation and concurrent interview was conducted with the Food and
Nutrition Services Director. Black dirt residue was observed on the kitchen hood. The Food and Nutrition
Services Director verified the finding and stated the kitchen staff were supposed to clean the hood weekly
for sanitation purposes and infection control.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055575
If continuation sheet
Page 7 of 8
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
055575
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pacific Haven Subacute and Healthcare Center
12072 Trask Ave.
Garden Grove, CA 92843
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 - Minimal harm
or potential for actual harm
Residents Affected - Few
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
observation, interview, medical record review, and facility P&P review, the facility failed to ensure the
medical record for one of 19 final sampled residents (Resident 64) was complete and systematically
organized. The facility failed to ensure Resident 64's respiratory rate and PIP were documented on the flow
sheet after each ventilator check as per the facility's P&P. This had the potential for the resident's care
needs not being met as their medical information was incomplete.
Findings:
Review of the facility's P&P titled Mechanical Ventilation Flowsheet (undated) showed services provided by
the respiratory care provider must be documented properly in the resident's medical record. Each ventilator
check will be recorded on the flow sheet with the following information as indicated, including the measured
(respiratory) rate and PIP.
On 11/15/22 at 0848 hours, Resident 64 was observed in bed with a tracheostomy tube in place and
connected to a mechanical ventilator.
Medical record review for Resident 64 was initiated on 11/15/22. Resident 64 was admitted to the facility on
[DATE] and readmitted on [DATE].
On 11/16/22 at 1421 hours, an interview and concurrent medical record review was conducted with RT 1.
Review of the Respiratory Evaluation dated 11/16/2022 at 0812 hours, failed to show documentation of
Resident 64's measured respiratory rate and PIP. RT 1 verified the finding and stated the PIP was important
because the ventilator high and low pressure alarms were set based on the PIP. Cross reference to F695.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055575
If continuation sheet
Page 8 of 8