F 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to ensure interventions (actions, treatments, procedures, or
activities designed to meet a residents goals) listed on a resident centered comprehensive care plan (a list
of resident specific problems, goals, and interventions) were specific to the care and services that would be
implemented for two of three sampled residents (Resident 1 and Resident 3) when, Resident 1 and
Resident 3's gastrostomy tube (G-tube; a thin tube surgically inserted into the stomach area to provide a
direct route for delivering nutrition, medications, and fluids) care plan intervention indicated to provide
dressing to the g-tube site as ordered, however there was no physician order for Resident 1 or Resident 3
in regards to g-tube skin care and dressing instructions and/or frequency.These failures had the potential
for Resident 1 and Resident 3 to experience skin breakdown and infection from the G-tube site.Findings: 1.
Review of Resident 1's clinical record titled, admission RECORD, indicated Resident 1 was admitted to the
facility with diagnosis including but not limited to .ENCOUNTER FOR ATTENTION TO GASTROSTOMY
[this diagnosis applies to routine tasks like cleansing, dressing changes, and managing the g-tube].During
a concurrent interview and record review on 9/24/25, at 3:43 p.m., with Licensed Nurse (LN) 1, Resident 1's
Order Summary Report, printed on 10/24/25, was reviewed. LN 1 confirmed there was no treatment order
for Resident 1's G-tube site. LN 1 stated the order should have been there, and it was part of the facility
policy to provide treatment to Resident 1's G-tube site every day. LN 1 further stated if the G-tube site does
not receive treatment there was a risk of infection and skin breakdown at the site.During a concurrent
interview and record review on 9/24/25, at 4:05 p.m., with the Director of Sub-Acute Services (DSAS;
provides more intensive medical services and therapy than a traditional nursing home but is less intensive
than acute (hospital) care) Resident 1's enteral feeding tube (also known as tube feeding, is a way of
sending nutrition right to the stomach or small intestine) care plan, dated 10/24/24, was reviewed. The
DSAS verified Resident 1's care plan indicated to monitor the skin around the g-tube site, provide skin care,
and dressing changes as ordered. The DSAS further stated it was her expectation for Resident 1 to have a
physician treatment order that included g-tube treatment instructions.2. Review of Resident 3's clinical
record titled, admission RECORD, indicated Resident 3 was admitted to the facility with diagnosis including
but not limited to .ENCOUNTER FOR ATTENTION TO GASTROSTOMY.During a concurrent interview and
record review on 9/25/25, at 3:07 p.m., with Licensed Nurse (LN) 2, Resident 1's, Order Summary Report,
with a printed date of 10/25/25, was reviewed. LN 2 verified Resident 3 was readmitted to the facility on
[DATE] and Resident 3 had no order for treatment for Resident 3's G-tube site until today, 9/25/25. LN 2
stated that without a treatment order for the g-tube, Resident 3 was at risk for skin breakdown and infection
of the G-tube site.During a concurrent interview and record review on 9/25/25, at 4 p.m., with the DSAS,
Resident 3's enteral feeding care plan, dated 3/4/23, and Order Summary Report, with a printed date of
10/25/25, was
(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 5
Event ID:
055735
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
055735
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Delta Oaks Post Acute
6940 Pacific Avenue
Stockton, CA 95207
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 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
reviewed. The DSAS verified Resident 3's enteral feeding care plan indicated interventions to change
Resident 3's dressing at the stoma site (an artificial opening created through surgery on the stomach) per
doctor's orders and to clean the stoma site as ordered/per facility protocol. The DSAS also verified Resident
3 did not have an order to change the dressing at the G-tube site or an order to clean the site. The DSAS
stated care plans provide interventions to situations that were resident specific. The DSAS further stated it
was important to follow the care plan to prevent infection.During an interview on 9/25/25, at 5:05 p.m., with
the Administrator (ADM), the ADM stated it was her expectation that care plans would be followed. The
ADM further stated it was important to follow the care plan to stay consistent with resident care.During a
review of the facility's policy and procedure (P&P) titled, CARE PLAN COMPREHENSIVE, dated 8/25/21,
the P&P indicated, .Each resident's comprehensive care plan is designed to. incorporate identified problem
areas.aid in preventing or reducing declines in the resident's functional status and/or functional levels.reflect
currently recognized professional standards of practice for problem areas and conditions .
Event ID:
Facility ID:
055735
If continuation sheet
Page 2 of 5
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
055735
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Delta Oaks Post Acute
6940 Pacific Avenue
Stockton, CA 95207
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 0688
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide appropriate care for a resident to maintain and/or improve range of motion (ROM), limited ROM
and/or mobility, unless a decline is for a medical reason.
Based on interview and record review, the facility failed to ensure appropriate treatment and services were
provided to prevent potential further decline in range of motion (ROM; the extent to which a joint can move
through its entire range of motion without pain or restrictions) for one of three sampled residents (Resident
1), when Resident 1's ordered Restorative Nursing Program (program to help ensure that residents retain
the skills gained in physical therapy and prevent declines that can impact the quality of a resident's life) to
provide passive range of motion (PROM; when another person or a machine moves a patient's limb or joint
through its full range of motion without the patient's active muscle contraction or effort) to Resident 1's
bilateral lower extremities (BLE; both legs) was discontinued on 2/5/25 without an updated referral from the
therapy department. This failure had the potential to result in decreased ROM for Resident 1 and for
Resident 1's contractures (a body part that gets stuck in a bent or shortened position because of
permanent tightening of muscles, tendons, ligaments, or skin that prevents a body part, most often a joint,
from moving freely) to worsen.Findings:Review of Resident 1's functional mobility (a person's capacity to
move safely and independently to perform activities of daily living (ADLs) such as walking, standing, sitting,
and transfers between surfaces) care plan, initiated 4/21/25, in the section titled Focus, indicated .[Resident
1] exhibits or is at risk for alterations in functional mobility related to contracture deformity [a fixed tightening
of muscle, tendons, ligaments, or skin that prevents normal movement of the associated body part]: Prevent
and Treatment: B [bilateral; both sides] UE/LE [upper extremity (arm)/lower extremity (leg)] contractors. In
the section titled Goals, indicated, .[Resident 1] will not have a decrease in ROM times 90 days.[Resident 1]
will have no increase in contractures X [times] 90 day [sic].A review of Resident 1's Minimum Data Set
(MDS, an assessment tool), in the section titled, Section GG - Functional Abilities, dated 8/3/25, indicated
Resident 1 was dependent on staff for all care needs including eating, toileting, bathing, personal hygiene,
and dressing.During a concurrent interview and record review on 9/24/25, at 11:28 a.m., with Restorative
Nurse Assistant (RNA) 1, Resident 1's document titled, RNA Orders & Referral Form, dated 12/6/24, was
reviewed. Review of Resident 1's RNA order, signed by the Director of Rehab (DOR), indicated to provide
.Passive ROM. [checked box] RNA for PROM to BUE & BLE.Non verbal [unable to speak], increase risk of
contracture related to immobility [unable to move on own], ROM. RNA 1 verified that this was Resident 1's
most recent referral for RNA services and stated Resident 1 was currently only receiving PROM therapy for
bilateral upper extremities three times a week. RNA 1 further stated that Resident 1 used to receive PROM
for BUE and PROM for BLE but stopped receiving BLE PROM between February and March of this year
(2025). During a concurrent interview and record review on 9/25/25, at 1:15 p.m., with the Director of
Nursing (DON), Resident 1's physician orders were reviewed. The DON verified Resident 1's physician
order for BLE PROM three times a week was discontinued on 2/5/25. The DON stated the facility should
have continued both BUE and BLE PROM therapy and Resident 1's order for BLE PROM should not have
been discontinued without a new referral from therapy. The DON further stated that without receiving the
BLE PROM Resident 1 was at risk of experiencing worsening contractures and potentially pain associated
with the joints and immobility.During an interview on 9/25/25, at 2:05 p.m., with Physical Therapy Assistant
(PTA) 1, PTA 1 stated Resident 1 would not be able to maintain range of motion or mobility without BLE
PROM. PTA 1 noted that Resident 1 was at risk for worsening contractures and potential discomfort.During
a review of Resident 1's document titled, Documentation Survey Report V2 for the months of 12/24 to 8/25
indicated Resident 1 last received BLE PROM on 2/13/25.During a review of the facility's policy and
procedure
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055735
If continuation sheet
Page 3 of 5
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
055735
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Delta Oaks Post Acute
6940 Pacific Avenue
Stockton, CA 95207
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 0688
(P&P) titled, Restorative Nursing Services, dated 7/17, the P&P indicated, .Residents will receive
restorative nursing care as needed to help promote optimal safety and independence.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055735
If continuation sheet
Page 4 of 5
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
055735
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Delta Oaks Post Acute
6940 Pacific Avenue
Stockton, CA 95207
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 0693
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Ensure that feeding tubes are not used unless there is a medical reason and the resident agrees; and
provide appropriate care for a resident with a feeding tube.
Based on interview and record review, the facility failed to ensure a physician order was in place to indicate
the appropriate care of a gastrostomy tube feeding (G-tube; a thin tube surgically inserted into the stomach
area to provide a direct route for delivering nutrition, medications, and fluids) for 2 of the 3 sampled
residents (Resident 1 and Resident 3) to prevent potential complications of the feeding tube when,
Resident 1 and Resident 2 did not have a physician treatment order to indicate the care needed for the
G-tube site.This failure had the potential for Resident 1 and Resident 3 to experience skin breakdown and
infection at the G-tube site.Findings:1. Review of Resident 1's clinical record titled, admission RECORD,
indicated Resident 1 was admitted to the facility with diagnosis including but not limited to .ENCOUNTER
FOR ATTENTION TO GASTROSTOMY [this diagnosis applies to routine tasks like cleansing, dressing
changes, and managing the g-tube].During a concurrent interview and record review on 9/24/25, at 3:43
p.m., with Licensed Nurse (LN) 1, Resident 1's Order Summary Report, printed on 10/24/25, was reviewed.
LN 1 confirmed there was no treatment order for Resident 1's G-tube site. LN 1 stated the order should
have been there, and it was part of the facility policy to provide treatment to Resident 1's G-tube site every
day. LN 1 further stated if the G-tube site does not receive treatment there was a risk of infection and skin
breakdown at the site.During an interview on 9/24/25, at 4:05 p.m., with the Director of Sub-Acute Services
(DSAS; provides more intensive medical services and therapy than a traditional nursing home but is less
intensive than acute (hospital) care), the DSAS stated it was her expectation for Resident 1 to have a
physician treatment order that included g-tube treatment instructions.A review of Resident 1's, Treatment
Administration Record, dated 8/24, indicated there was no documented evidence that Resident 1 received
treatment to the G-tube site upon readmission to the facility on 8/9/24.2. Review of Resident 3's clinical
record titled, admission RECORD, indicated Resident 3 was admitted to the facility with diagnosis including
but not limited to .ENCOUNTER FOR ATTENTION TO GASTROSTOMY.During a concurrent interview and
record review on 9/25/25, at 3:07 p.m., with Licensed Nurse (LN) 2, Resident 1's, Order Summary Report,
with a printed date of 10/25/25, was reviewed. LN 2 verified Resident 3 had no active order for treatment for
Resident 3's G-tube site from 8/20/25, until today, 9/25/25. LN 2 stated that without a treatment order for the
g-tube, Resident 3 was at risk for skin breakdown and infection of the G-tube site.During a concurrent
interview and record review on 9/25/25, at 4 p.m., with the DSAS, Resident 3's Order Summary Report,
with a printed date of 10/25/25, was reviewed. The DSAS verified Resident 3 did not have an order to
change the dressing at the G-tube site or an order to clean the site. The DSAS stated if Resident 3's G-tube
site did not have a treatment order Resident 3 was at risk for infection and skin breakdown at the G-tube
site.During a review of the facility's policy and procedure (P&P) titled, Enteral Feedings [a method of
providing nutrition directly into the gastrointestinal (GI; includes stomach and intestines) tract through a
tube] - Safety Precautions, dated 11/18, the P&P indicated, .The facility will remain current in and follow
accepted best practices in enteral nutrition.Keep the skin around exit site clean, dry and lubricated.
Event ID:
Facility ID:
055735
If continuation sheet
Page 5 of 5