F 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
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.
Based on interview and record review, the facility failed to ensure 4 of 24 sampled residents (Resident 7,
Resident 32, Resident 53, Resident 90) were offered an advance directive (a legal document where a
competent adult specifies their future medical care wishes in the event they cannot communicate them
themselves, often due to illness or injury). This failure had the potential to result in the residents' medical
wishes not being honored.Findings:During a review of Resident 7's admission record (AR), the AR
indicated Resident 7 was admitted in November 2025 with several diagnosis including aftercare following
surgical amputation (surgical removal of part or all of a body part).During a review of Resident 32's AR, the
AR indicated Resident 32 was admitted in November 2025 with several diagnosis including encephalopathy
(a condition where brain dysfunction occurs due to a chemical imbalance in the body, often triggered by
systemic illnesses or organ dysfunction). During a review of Resident 53's AR, the AR indicated Resident
53 was admitted in December 2025 with several diagnosis including severe protein calorie
malnutrition.During a review of Resident 90's AR, the AR indicated Resident 90 was admitted in December
2025 with several diagnosis including acute respiratory failure with hypoxia (low levels of oxygen in tissues
and organs). During a review of Resident 7, Resident 32, Resident 53, and Resident 90 ‘s clinical records,
the clinical records did not have an advance directive or documentation that indicated an advance directive
was offered. During a concurrent interview and record review on 1/8/26 at 2:06 p.m. with Social Services
Director (SSD), SSD confirmed Resident 7, Resident 32, Resident 53, and Resident 90 did not have an
advance directive or documentation that indicated an advance directive was offered. SSD stated the
expectation was for advance directives to be offered at admission. SSD further stated there should have
been documentation that indicated an advance directive was offered if residents did not have an advance
directive. SSD further stated there was a risk for residents' medical wishes to be unclear when an advance
directive was not available. During a review of the facility's policy and procedure (P&P) titled, Advance
Directives revised 2/25, the P&P indicated, .it is the policy of this facility to inform and provide written
information to all adult residents concerning the right to accept or refuse medical or surgical treatment and,
at the resident's option, formulate an advance directive Prior to, upon, or immediately after admission, the
facility staff will ask residents, and/or their family members, about the existence of any advance
directives.Should the resident indicate that he or she has issued advance directives about his/her care and
treatment, the facility will require that a copy of such directives be included in the medical record.
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 7
Event ID:
055014
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
055014
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/09/2026
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairfield Post-Acute Rehab
1255 Travis Blvd
Fairfield, CA 94533
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 0605
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Prevent the use of unnecessary psychotropic medications or use medications that may restrain a resident's
ability to function.
Based on interview and record review, the facility failed to ensure one of 24 sampled residents (Resident 9)
was free of unnecessary psychotropic medications (any drug that affects behavior, mood, thoughts or
perception) when Resident 9 did not receive a psychiatric evaluation to determine if their psychotropic
medication should be continued.This failure had the potential to result in the use of an unnecessary
psychotropic medication that could cause adverse consequences.During a review of Resident 9's
admission record (AR), the AR indicated Resident 9 was admitted to the facility in November 2025 with
multiple diagnosis including dementia (a progressive state of decline in mental abilities). Resident 9's AR
did not indicate a diagnosis of schizophrenia (a mental illness that is characterized by disturbances in
thought) and bipolar disorder (sometimes called manic-depressive disorder; mood swings that range from
the lows of depression to elevated periods of emotional highs). During a review of Resident 9's physician's
orders dated 11/7/25, the physician's orders indicated Resident 9 was prescribed quetiapine (a
psychotropic medication that treats schizophrenia and bipolar disorder).During a review of Resident 9's
Initial Psychology Evaluation dated 11/26/25, the Initial Psychology Evaluation did not include a review of
quetiapine or address the reason for starting and continuing quetiapine.During an interview with
Neuropsychologist (NPSY) on 1/8/26 at 11:32 a.m., the NPSY confirmed she was the clinician that
evaluated Resident 9 on 11/26/25. The NPSY stated quetiapine was not reviewed during the Initial
Psychology Evaluation. The NPSY further stated I missed it (quetiapine) on the med (medication) list. The
NPSY confirmed Resident 9 did not have a diagnosis of schizophrenia or bipolar disorder.During an
interview on 1/9/25 at 10:20 a.m., with the Director of Nursing (DON), DON stated the expectation was for
NPSY to review the quetiapine during the Initial Psychology Evaluation on 11/26/25. DON acknowledged
the risk for mortality when Resident 9's quetiapine was not reviewed.During a review of the U.S. Food, Drug
and Administration (FDA) medication guide for quetiapine, revised 8/19, the FDA medication guide
indicated quetiapine increased the risk of death in elderly people with dementia.During a review of the
facility's policy and procedure (P&P) titled, Psychotropic Drug Use, revised 2/2025, the P&P indicated, .It is
the policy of this facility to ensure that residents who have not used psychotropic drugs are not given these
drugs unless the medication is necessary to treat a specific condition as diagnosed and documented in the
clinical record. Upon initial comprehensive assessment, SSD and/or nursing designee shall review new
admissions for.physician's orders for psychotropic medications. These residents will be referred to the
facility's Psychotropic Drug Review Committee and/or the Psychiatrist.
Event ID:
Facility ID:
055014
If continuation sheet
Page 2 of 7
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
055014
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/09/2026
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairfield Post-Acute Rehab
1255 Travis Blvd
Fairfield, CA 94533
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 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Many
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
Based on observation, interview, and record review, the facility failed to ensure medications were stored
properly, when an unlabeled loose pill and three labeled blister packs (a type of unit-dose packaging with
clear plastic bubbles (blisters) holding individual pills) were found on the bottom of a drawer and in the back
of the drawers for one out of five sampled medication carts. These failures had the potential for medication
error, misuse, or drug diversion.Findings: During an inspection of Medication Cart 5 on 1/6/26 at 12:20
p.m., one unlabeled loose pill and three labeled blister packs were found on the bottom of the drawer and
behind the drawers in the back of medication cart 5.During an interview on 1/6/26 at 9:48 a.m. with Nursing
Supervisor (NS), NS removed the pill found on the bottom of the drawer and confirmed there was 1 loose
pill. NS also confirmed there were three labeled blister packs found behind the drawer at the back of cart 5.
The NS stated the carts were cleaned regularly but admitted she did not think of looking behind the
drawers. The NS confirmed the loose pill or the misplaced medications in the back of the cart could have
led to a mediation error. During an interview on 1/6/26 at 1:29 p.m. with the Director of Nursing (DON), the
DON confirmed medications should not be loose in the drawers and medications should not be at the back
of the cart behind the drawers. The DON stated, the medication carts should be checked thoroughly, and
kept clean. The DON stated the loose pill and medications in the back of the cart could lead to a medication
error.During a review of the facility Policy and Procedure (P&P), titled, Storage of Medications, dated May
2022, the P&P indicated, Medications and biologicals are stored safely, securely, and properly .All
medications. are stored in the container with the pharmacy label.
Event ID:
Facility ID:
055014
If continuation sheet
Page 3 of 7
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
055014
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/09/2026
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairfield Post-Acute Rehab
1255 Travis Blvd
Fairfield, CA 94533
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 - Many
FORM CMS-2567 (02/99)
Previous Versions Obsolete
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 store cookware pans and
utensils in accordance with professional standards for food service safety when: Frying pans were stacked
wet while stored away; and, Ladles and cake slicer were found wet while stored in the drawer.These failures
had potential to cause food-borne illnesses in a highly susceptible population of 97 residents who received
food from the kitchen.Findings:During a concurrent initial tour observation and interview on 1/6/26 at 8:45
a.m. at the kitchen with the Certified Dietary Manager (CDM), several wet pans and ladles were stacked
and stored at the clean and ready-to-use storage areas as indicated below:6 frying pans- different sizes6
ladles - various sizes1 cake slicerThe CDM confirmed that the 6 frying pans, 6 ladles, and 1 cake slicer
were wet. CDM stated, the frying pans, ladles, and a cake slicer should have been completely air dried
before being stored away.During an interview on 1/8/26 at 10 a.m. with Registered Dietician (RD), the RD
stated, the expectation was: the frying pans and ladles including the cake slicer will be cleaned and air
dried before it is stored away.During a review of an undated facility's policy and procedure titled,
Dishwashing, indicated, .dishes are to be air dried in racks before stacking and storing.
Event ID:
Facility ID:
055014
If continuation sheet
Page 4 of 7
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
055014
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/09/2026
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairfield Post-Acute Rehab
1255 Travis Blvd
Fairfield, CA 94533
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 0813
Have a policy regarding use and storage of foods brought to residents by family and other visitors.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview and record review, the facility failed to store resident food in a safe and
sanitary manner in the refrigerators for residents for a census of 97 when:One opened bottle of soda stored
past their use by date,Two bottles of opened salad dressings, and one fruit spread found unlabeled,One
bag of loaf of bread was unlabeled, undated, and expired; and,Opened container of clam chowder with
expired use by date.These failures had the potential to cause foodborne illnesses in a vulnerable resident
population. Findings:During a concurrent observation and interview on 1/8/26 at 10:30 a.m. with Certified
Dietary Manager (CDM), several resident food items were found in the refrigerators for residents at Nursing
Station 1 and Nursing Station 2. The food items found were as follows:Nursing Station 1 refrigerator for
residents:One opened bottle of soda stored past their use by date 12/27/25.Two opened salad dressings,
and one fruit spread found unlabeled, undatedOpened Clam Chowder with use by date 1/7/26 and
unlabeled.Nursing Station 2 refrigerator for residents:One bag of loaf of bread was unlabeled, undated, and
expired.CDM confirmed the findings and stated her expectations were to have all residents' food be
labelled. CDM further stated, . staff must check the resident refrigerators every night and discard anything
that has expired or does not have any labels.During an interview on 1/8/26 at 11 a.m. with the Registered
Dietician (RD), RD stated, her expectations were for the staff to label the food received from home, the
date, and the location of the resident. RD further stated perishable food that has been opened must be
discarded after 3 days.During a review of the facility's policy and procedure titled, Foods Brought by Family
or Visitor, revised 2/2025, indicated, .all foods shall be labeled with the resident name, location, and
date.perishable prepared foods will be checked by nurse, dietary staff daily and discarded after 3 days of
storage.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055014
If continuation sheet
Page 5 of 7
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
055014
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/09/2026
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairfield Post-Acute Rehab
1255 Travis Blvd
Fairfield, CA 94533
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 0880
Provide and implement an infection prevention and control program.
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 proper infection prevention measures
were implemented for a census of 97 when:One facility staff did not sanitize the blood pressure
(BP-measures the force of blood against artery walls) cuff in between two residents (Resident 2 and
Resident 61).These failures had the potential to spread germs.Findings:A review of Resident 2's clinical
record indicated Resident 2 was admitted [DATE] with diagnosis that included Chronic Viral Hepatitis C (a
long term viral infection of the liver that leads to illness and can be spread by contact with the contaminated
blood), Immunodeficiency (the immune system can't effectively fight infections and diseases, leading to
frequent, severe infections and potentially cancer), Chronic Obstructive Pulmonary Disease (COPD-a
chronic lung disease causing difficulty in breathing).A review of Resident 61's clinical record indicated
Resident 61 was admitted [DATE] with diagnosis that included Immunodeficiency, and Pneumonia (an
infection/inflammation in the lungs).During a concurrent observation and interview on 1/6/26 at 8:47 a.m.,
9:01 a.m., and 9:14 a.m., respectively with Licensed Nurse (LN)1, LN 1 did not sanitize the BP cuff before,
after or in between taking the BP of Resident 2 and Resident 61. LN 1 stated, .we are supposed to sanitize
the blood pressure cuff after each use, but I forgot. LN 1 stated not sanitizing the BP cuff could spread
germs.During an interview on 1/6/26 at 12 p.m. with the Nursing Supervisor (NS), the NS stated, the BP
cuff and machine needed to be wiped down in between each resident use. The NS stated that not sanitizing
can lead to spreading germs.During an interview on 1/6/26 at 1:29 p.m., with the Director of Nursing
(DON), the DON stated the expectation was for the BP cuff to be sanitized in between each resident use to
prevent the spread of germs.During a concurrent interview on 1/7/26 at 9:56 a.m. with the Infection
Preventionist (IP) and Director of Staff Development IP Consultant (DSD IP), the IP and DSD IP stated the
expectation for sanitizing the BP cuff was to sanitize the cuff in between each resident use.A review of the
facility's policies and procedures (P&P) titled, Infection Control Program, revised 2/2025, indicated,
.Patient-care equipment (e.g., blood pressure cuffs).clean and disinfect such equipment before use on
another patient.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055014
If continuation sheet
Page 6 of 7
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
055014
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/09/2026
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairfield Post-Acute Rehab
1255 Travis Blvd
Fairfield, CA 94533
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 0912
Level of Harm - Potential for
minimal harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Provide rooms that are at least 80 square feet per resident in multiple rooms and 100 square feet for single
resident rooms.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review, the facility failed to ensure 28 multiple-resident rooms (rooms 1-9,
11-13, 15-21, 28-35, 37) met the required 80 square feet (sq. ft.) per resident when the following rooms
were measured as:room [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft.
per personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personroom [ROOM NUMBER] at 75.5 sq. ft. per personroom [ROOM NUMBER] at 75.5 sq. ft. per
personThese failures had the potential to negatively affect the residents' quality of life and result in
inadequate space for the provision of care.During observations made throughout the survey in the rooms
with three resident occupancies, the space was adequate to store assistive devices in the rooms (such as
wheelchairs and/or walkers) and to facilitate provision of care and needs.During an interview on 1/7/26 at
8:22 a.m., a resident in room [ROOM NUMBER] stated he could get around his room without issues when
wheelchair and trashcans were not blocking pathways to bathroom.During an interview on 1/7/26 at 8:29
a.m., a resident in room [ROOM NUMBER] stated she had no concerns or issues with the size of the
room.During an interview on 1/8/26 at 12:59 p.m. with Licensed Nurse 2 (LN 2), LN 2 stated there were no
issues with room sizes. LN 2 further stated there was enough room to do her job. LN 2 further stated
wheelchairs and trash cans must be moved to accommodate a Hoyer lift while transferring residents.During
an interview on 1/8/26 at 1:05 p.m. with Certified Nursing Assistant 2 (CNA 2), CNA 2 stated if there was no
clutter and resident items were organized, there was enough space in the rooms for her to do her
job.During an interview on 1/8/26 at 1:25 p.m., a resident in room [ROOM NUMBER] stated she had no
issues moving around in her room.The Department recommends continuation of the waiver for the
above-mentioned rooms.
Event ID:
Facility ID:
055014
If continuation sheet
Page 7 of 7