F 0727
Level of Harm - Potential for
minimal harm
Residents Affected - Some
Have a registered nurse on duty 8 hours a day; and select a registered nurse to be the director of nurses on
a full time basis.
Based on interview and record review, this requirement was not met when the facility failed to obtain the
services of a registered nurse for eight consecutive hours, seven days a week. This had the potential to
adversely affect residents' care, which could lead to potential negative clinical outcomes.
Findings:
A review of the facility's Registered Nurse (RN) staffing/schedule documentation from the period of 11/1/24
to 11/30/24 indicated that the RN working as Director of Nursing (DON) was scheduled to work weekdays
(Monday through Friday) leaving six weekend days (11/2, 11/3, 11/9, 11/10, 11/23, and 11/30/24)
uncovered during this four-week time period. There are two days (11/28, and11/29/24) when the DON had
time off.
On 11/5/24 at 7 am, during an interview with the facility's Chief Nursing Officer (CNO), the CNO indicated
the facility had requested the federal waiver for RN coverage, indicating a reduction in the required
registered nurses' hours from 56 hours a week to 40 hours a week to be renewed this year. We have the
waiver and will have it renewed again.
On 11/6/24 at 9:30 am, during the resident council meeting (a meeting for residents to voice concerns
regarding living in a facility), there were no complaints of staffing issues. Four of four confidentially
interviewed residents did not have staffing concerns.
During an interview and concurrent record review with the Director of Nursing (DON) on 11/06/24 at 10:45
am, the DON confirmed there was no RN coverage on weekends. During review of the staffing schedule
the DON stated, I am here weekdays but there isn't an RN on weekend days. An RN is available from the
acute hospital, down the connecting hallway, if needed.
On 11/6/24 at 2:10 pm, during an interview, Licensed Vocational Nurse A (LN) A stated, On weekends we
can call the DON or if really urgent, we can get an RN from either Med/Surg (the medical surgical unit) or
the ER. We do that after hours too because there is only an LVN at night for the 12-hour shift. LN A had no
concerns regarding the weekend RN staffing.
The survey team found no negative outcomes related to continuing this federal waiver for RN coverage, and
recommends it be continued.
.
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 4
Event ID:
555022
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
555022
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/07/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Seneca District Hospital D/P Snf
130 Brentwood Dr
Chester, CA 96020
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 - Some
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 that blood sugar testing
equipment was dated when opened and that the glucometers (a machine used to test blood sugar), was
calibrated (a control test to ensure the glucometer readings are accurate) when:
a. Two vials of glucometer control test vials were not dated when opened, or when the solution was to be
discarded.
b. Two bottles of glucometer test strips were not dated when opened, or when they were to be discarded.
c. Facility failed to perform quality control (QC) calibration checks daily on glucometers.
These failures could lead to inaccurate blood sugar test results due to using outdated, inaccurate, and less
effective testing equipment and supplies, which could result in negative clinical outcomes for the residents.
Findings:
A review of the facility's policies and procedures (P&P) titled, Glucose Testing Machine: Care and Use of,
dated 6/19/24, indicated, before using the glucometer and testing a resident's blood sugar, facility staff
would Verify that QC was performed and within expected limits.
A review of the undated document titled, SNF Meeting (notes regarding education reviewed and provided to
facility staff during a staff meeting), indicated, facility staff were perform daily glucometer QC checks. The
document indicated, The test solution and strips must have an outdate placed on the outside. Expiration
date for the control solution is three (3) months from opening, test strips are six (6) months from opening.
During a concurrent observation, interview, and record review on 11/6/24 at 2:30 pm, located at the
glucometer storage area in the nurse's station, with Licensed Nurse (LN) A, two bottles of glucometer
control test vials, two bottles of glucometer test strips, and the Equipment Maintenance Record, dated
6/1/24 through 11/5/24 were reviewed and reflected the following;
a. LN A stated, when the control test vials were opened, the expectancy was that LN dated the control test
vials with the date it was opened and the date they were to be discarded. LN A confirmed, both control test
vials were not dated with the opened or discarded dates and should have been. LN A reviewed the
manufacturer's recommendations (MR) titled, Nova StatStrip Glucose Control Solution, dated, 1/1/22, and
stated the MR indicated, 'the control test vials were to be discarded three months after opening or the
expiration date, which ever date was sooner.'
b. LN A stated, when the glucometer control test strips were opened, the expectancy was that LN dated the
control test strips with the date they were was opened and the date they were to be discarded. LN A
confirmed, both bottles of control test strips were not dated with the opened or discarded dates and should
have been. LN A reviewed the MR titled, StatStrip Glucose Hospital Test Strips, dated 1/1/22, and stated,
the MR indicated the glucometer test strips were to be discarded six months
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555022
If continuation sheet
Page 2 of 4
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
555022
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/07/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Seneca District Hospital D/P Snf
130 Brentwood Dr
Chester, CA 96020
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
after opening or the expiration date, which ever date was sooner.
Level of Harm - Minimal harm
or potential for actual harm
c. LN A reviewed the Equipment Maintenance Record, dated 6/1/24 through 11/5/24 and stated the night
shift was to perform a QC check on the glucometer every night. LN A confirmed multiple missing entries
located on the, Equipment Maintenance Record, eight for the month of June, 12 for the month of July, six
for the month of August, three for the month of September, 9 for the month of October, and one in the first 5
days of November. The Equipment Maintenance Record, included instructions to discard control solutions 3
months after opening.
Residents Affected - Some
On 11/6/24 at 2:45 pm, during an observation and interview, the Chief Nursing Officer (CNO), confirmed
two bottles of glucometer control test vials and two bottles of glucometer test strips did not have opened or
discarded dates and should have. CNO reviewed the, Equipment Maintenance Record, dated 6/1/24
through 11/5/24, and confirmed there were multiple missing quality calibration checks for the glucometers,
and stated the night shift was responsible for performing the glucometer QC test every night.
.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555022
If continuation sheet
Page 3 of 4
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
555022
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/07/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Seneca District Hospital D/P Snf
130 Brentwood Dr
Chester, CA 96020
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 0804
Ensure food and drink is palatable, attractive, and at a safe and appetizing temperature.
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 observe the meal preferences of one of eight
sampled residents when Resident 9 was served brussel sprouts. This failure had the potential to reduce
intake of nutrients, weight loss and have negative clinical outcomes.
Residents Affected - Few
Findings:
A review of the facility's undated policy and procedure titled, Skilled Nursing Facility Food Preferences,
indicated, the facility would take into consideration resident food preferences.
A review of an untitled and undated record indicated, Resident 9 was admitted to the facility on [DATE] with
the diagnoses of type 2 diabetes (high blood sugar) and major depressive disorder (a sad mood).
A review of the annual (yearly) Minimum Data Set (MDS, an assessment tool), dated 10/8/24, Section C,
indicated, Resident 9 had a Brief Interview for Mental Status (an assessment that tested a resident's ability
to recall information and memory. The test was scored from 0-15 where 0 meant the resident was not able
to remember and 15 meant the resident had intact memory) and scored a 14.
During a concurrent observation and interview on 11/4/24 at 12:04 pm, Licensed Nurse (LN) B was
observed outside of the resident dining area checking resident lunch trays. LN B stated, when meal trays
come out, LNs checked the meal trays to ensure the residents received the correct diet, food preferences,
and resident food allergies. During the observation, LN B checked all the lunch trays prior to the residents
being served.
During a concurrent observation, interview, and record review, on 11/4/24 at 12:09 pm, LN B provided
Resident 9 with her lunch tray. When the lid was removed from the lunch plate, Resident 9's smile changed
to a frown, she appeared upset, with eyebrows scrunched together. Resident 9 cursed loudly and, having a
dislike of brussel sprouts stated, I tell them all the time and I keep getting them. Resident 9's tray card (a
card that indicated a resident's diet, allergies, and dislikes) was reviewed and indicated Resident 9 had a
dislike of brussel sprouts. LN B apologized to Resident 9 and stated, I forgot to have the brussel sprouts
removed.
During a concurrent observation, interview, and record review, on 11/6/24 at 11:49 am, the dietary staff was
observed plating resident lunches. A document that contained resident food dislikes was observed, taped to
a cupboard door near the tray line (where food was placed on plates). The document indicated, Resident 9
did not like brussel sprouts. [NAME] affirmed remaking the resident dislike food list a few days ago and
forgetting to add Resident 9's dislike of brussels sprouts to the list. [NAME] stated, the x, indicating a dislike
of brussel sprouts was added to the document on 11/4/24 after lunch was served.
During a concurrent interview and record review on 11/6/24 at 2:42 pm, Resident 9's Food Preferences,
dated 9/28/23, was reviewed with the Registered Dietician (RD). The RD stated, the 'Food Preferences'
indicated Resident 9 did not like brussel sprouts and confirmed, Resident 9 was served brussel sprouts at
lunch on 11/4/24.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555022
If continuation sheet
Page 4 of 4