F 0558
Reasonably accommodate the needs and preferences of each resident.
Level of Harm - Minimal harm
or potential for actual harm
Based on review of select facility policy, observations, and resident and staff interviews, it was determined
that the facility failed to ensure that residents had reasonable and safe access to operate their over-the-bed
lighting for four residents out of 21 residents reviewed (Residents 32, 50, 9, and 41). Findings include: The
facility policy titled Environment last reviewed by the facility on October 1, 2025, indicated that the facility
shall provide extra lighting to provide sufficient light to assist residents with tasks such as reading, and
provide lighting for residents who need to find their way from the bed to the bathroom at night. During
observations conducted on November 13, 2025, at 9:45 AM, it was noted that Residents 32, 41 and 9 had
over-the-bed lighting fixtures; however, each fixture had a pull cord measuring two inches in length, making
the light inaccessible to residents. An interview with Resident 41during the observation revealed that she
was unable to reach the over-the-bed light while in bed or while seated in the wheelchair. She stated, I
would really like to. In fact, I need to. I get up a lot during the night and take myself to the bathroom, and I
should have a light on so I can see what I'm doing. During an observation of Resident 50's room on
November 13, 2025, at 10:15 AM, it was revealed that although an extension chain had been attached to
the over-the-bed light, the resident's bed was positioned too far away for her to reach it. Resident 50
explained that the cord was not long enough for her to access from either the bed or wheelchair. She
reported that her physical limitations, including upper body contractures (permanent tightening of muscles,
tendons, ligaments or skin that limits normal movement) and deformities, further limited her reach. She
stated, I like to read at night. When I'm done, I need to call the staff to turn it off. Sometimes I fall asleep
before they come to turn it off and they wake me up to ask what I need. If they could give me a long enough
cord, that would be very helpful. During an interview with the Nursing Home Administrator on November 14,
2025, at 9:30 AM, it was confirmed that the facility failed to ensure resident access to operate over-the-bed
lights for multiple residents, representing a failure to accommodate individual needs and preferences. 28
Pa. Code: 211.10(d) Resident care policies. 28 Pa. Code: 211.12(d)(3)(5) Nursing services.
Residents Affected - Some
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 13
Event ID:
395581
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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 0686
Provide appropriate pressure ulcer care and prevent new ulcers from developing.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on a
review of clinical records, select facility policy, observations, and staff interviews, it was determined the
facility failed to consistently implement measures planned to prevent the development of pressure sores for
one resident out of 21 residents sampled (Resident 76).Findings include: According to the US Department
of Health and Human Services, Agency for Healthcare Research & Quality, the pressure ulcer best practice
bundle incorporates three critical components in preventing pressure ulcers: comprehensive skin
assessment, standardized pressure ulcer risk assessment, and care planning and implementation to
address the areas of risk. The American College of Physicians (ACP) is a national organization of internists
who specialize in the diagnosis, treatment, and care of adults. The largest medical specialty organization
and second-largest physician group in the United States, Clinical Practice Guidelines indicate that the
treatment of pressure ulcers should involve multiple tactics aimed at alleviating the conditions contributing
to ulcer development (i.e., support surfaces, repositioning, and nutritional support); protecting the wound
from contamination and creating and maintaining a clean wound environment; promoting tissue healing via
local wound applications, debridement, and wound cleansing; using adjunctive therapies; and considering
possible surgical repair. A review of the facility policy titled Wound Management/Pressure Reduction, last
reviewed October 1, 2025, indicated it is the policy of the facility to assess each resident's potential for skin
breakdown based on clinical risk factors, and the plan of care will be established to address prevention and
treatment as needed, and that all residents will have a prevention or specialty mattress as needed. Further
review revealed to apply pressure-relieving boots, heel/elbow protectors, or heel elevators as
recommended by the wound nurse practitioner, therapist, or physician. A review of the clinical record
revealed that Resident 76 was admitted to the facility on [DATE] with diagnoses that included methicillin
susceptible staphylococcus aureus (MSSA, a type of bacterial infection caused by staphylococcus aureus
bacteria that are susceptible to treatment with methicillin and other beta-lactam antibiotics) after having a
right knee replacement surgery on October 7, 2025, and required use of a right knee immobilizer (a brace
that holds the knee joint straight to prevent bending). A review of an admission Minimum Data Set
assessment (MDS, a federally mandated standardized assessment process conducted periodically to plan
resident care) dated November 10, 2025, revealed that Resident 76 was cognitively intact with a BIMS
score of 15 (Brief Interview for Mental Status, a tool within the Cognitive Section of the MDS that is used to
assess the resident's attention, orientation, and ability to register and recall new information; a score of
13-15 indicates cognition is intact). A review of the resident's care plan, initiated November 7, 2025,
revealed a potential skin breakdown related to alteration in mobility due to recent surgery and that Resident
76 had actual skin breakdown caused by pressure with the presence of a Stage II ulcer ( partial-thickness
skin loss with loss of the outermost layer of the skin, usually shallow with a pink to red wound base) to the
coccyx (the small bone at the very bottom of the spine) noted on admission. A Braden Scale for Predicting
Pressure Sore Risk form on admission dated November 7, 2025, identified Resident 76 as being at
moderate risk for pressure injury development. Physician's orders dated November 8, 2025, included a
pressure-reducing mattress for the bed, a pressure-reducing cushion for the chair, and a Prevalon boot (a
medical device designed to protect the heels and prevent pressure ulcers) for the right lower extremity while
in bed. An observation of Resident 76 on November 12, 2025, at 11:00 AM revealed the resident lying
down in bed wearing a right knee immobilizer, without the presence of a Prevalon boot on the right lower
extremity. Observation of Resident 76's room revealed no Prevalon boot. A second observation on
November 13, 2025, at 9:00 AM
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395581
If continuation sheet
Page 2 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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 0686
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
revealed Resident 76 was lying down in bed wearing a right knee immobilizer, without the presence of a
Prevalon boot on the right lower extremity, which was confirmed by Employee 6, Licensed Practical Nurse.
An interview with the resident revealed he never had a Prevalon boot placed on his right lower extremity
since being admitted to the facility. A review of Resident 76's treatment administration record (TAR) from
November 2025 indicated the Prevalon boot on the right lower extremity was documented as being on the
resident from November 8, 2025, through November 12, 2025, with no documentation of refusals noted.
During an interview with the Nursing Home Administrator on November 13, 2025, at 9:45 AM, it was
confirmed the facility did not consistently implement the planned interventions to prevent a right heel
pressure ulcer for Resident 76. 28 Pa. Code 201.18(b)(1) Management 28 Pa. Code 211.10(d) Resident
care policies. 28 Pa. Code 211.12 (d)(1)(3)(5) Nursing services.
Event ID:
Facility ID:
395581
If continuation sheet
Page 3 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
clinical record review, review of select facility policy, and resident and staff interviews, it was determined the
facility failed to consistently provide restorative nursing services as planned to maintain mobility to the
extent possible for one resident out of 21 residents sampled (Resident 2). Findings include: A review of the
facility policy titled Restorative Nursing Program, last reviewed by the facility on October 1, 2025, revealed it
is the facility's policy to assist residents in maintaining or achieving the highest level of functioning through
the intervention of restorative nursing. The policy indicates therapy will develop and recommend a plan of
care, certified nursing aides are responsible for ensuring the program is performed per the plan of care, and
the restorative nurse or designee will be responsible for overseeing the restorative aides. A clinical record
review revealed that Resident 2 was admitted to the facility on [DATE], with diagnoses that include chronic
kidney failure (gradual loss of kidney function) and neuropathy (damage to the peripheral nervous system,
which carries signals between the brain and the rest of the body). A review of an admission Minimum Data
Set assessment (MDS, a federally mandated standardized assessment process conducted periodically to
plan resident care) dated September 7, 2025, revealed that Resident 2 was cognitively intact with a BIMS
score of 14 (Brief Interview for Mental Status, a tool within the Cognitive Section of the MDS that is used to
assess the resident's attention, orientation, and ability to register and recall new information; a score of 13
to 15 indicates cognition is intact). A physical therapy Discharge summary dated [DATE], revealed
discharge recommendations for Resident 2 to receive 24-hour care and a functional maintenance program
(a program designed to help the resident maintain their current level of physical ability and prevent decline
through routine, targeted exercises or activities) and restorative nursing program(a nursing-led program
providing ongoing, repetitive exercises to help the resident maintain or improve physical function after
skilled therapy ends). A review of Resident 2's plan of care revealed a focus indicating he would receive a
restorative nursing program with active range of motion (AROM exercises in which the resident moves their
own joints through their available range without assistance)) and passive range of motion (PROM exercises
in which staff move the resident's joints for them because the resident cannot move the joints
independently) initiated on September 29, 2025. The plan of care indicated Resident 2 would receive the
following exercises: (1) 15 left lower extremity (LLE) AROM hip flexion repetitions for two sets(2) 15
abduction and adduction repetitions for two sets(3) 15 knee flexion and extension repetitions for two sets(4)
15 right lower extremity (RLE) AROM and PROM hip flexion repetitions for two sets(5) 15 abduction and
adduction repetitions for two sets(6) 15 knee flexion and extension repetitions for two sets During an
interview on November 12, 2025, at 11:20 AM, Resident 2 indicated that he no longer receives therapy
services at the facility. He explained that he does not receive any restorative nursing program interventions
such as passive range of motion (PROM) or active range of motion (AROM) exercises. Resident 2 indicated
he has not had any restorative nursing exercises for over a month. A review of Resident 2's documentation
survey report (an electronic health record that indicates tasks completed for resident care) dated November
2025, revealed the facility provided the resident with 15 to 30 minutes of active range of motion exercises
on each day from November 1, 2025, through November 13, 2025. The document indicated that Employee
3, Nurse Aide (NA), provided Resident 2 with 15 minutes of active range of motion exercise on November
13, 2025, at 11:28 AM. During an interview on November 13, 2025, at 11:32 AM, Resident 2 indicated that
he had not received any restorative nursing interventions that morning and he further stated he had not
received any
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395581
If continuation sheet
Page 4 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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
FORM CMS-2567 (02/99)
Previous Versions Obsolete
exercises with staff since therapy ended over a month ago. During an interview on November 13, 2025, at
11:44 AM, Employee 3 (Nursing Assistant) confirmed she did not provide Resident 2 with the 15 minutes of
active range of motion exercises identified in his care plan. She acknowledged she documented the
intervention as completed in the resident's medical record even though it had not been provided. Employee
3 confirmed it is not the facility's policy for staff to document completion of care plan interventions before
they are carried out. During an interview on November 13, 2025, at 12:05 PM, the findings were reviewed
with the Director of Nursing. The Director of Nursing confirmed it is not the facility's policy for staff to
document care plan interventions as completed prior to implementation. The Director of Nursing
acknowledged the facility did not ensure that Resident 2's restorative nursing program interventions were
implemented as outlined in his plan of care and did not ensure that Resident 2 was provided with the
services needed to maintain mobility to the extent possible. 28 Pa. Code: 211.5(f)(ix) Medical records. 28
Pa. Code: 211.10(c) Resident care policies. 28 Pa Code 211.12(d)(3)(5) Nursing services.
Event ID:
Facility ID:
395581
If continuation sheet
Page 5 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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 a
review of clinical records, select facility policy, and resident and staff interviews, it was determined that the
facility failed to timely identify weight loss, failed to ensure weekly weights were obtained as required by
policy for prompt intervention for two of 21 sampled residents (Residents 15 and 22), and failed to
implement individualized nutritional support measures based on a resident's stated preferences to maintain
or improve nutritional parameters for one resident (Resident 8) out of three sampled residents for weight
loss. Findings include: A review of the facility's policy titled Weighing Residents/Reporting Significant Weight
Changes, last reviewed by the facility on October 1, 2025, revealed it is the facility policy to monitor weights
on all residents. The policy indicated the facility will investigate, report, and appropriately intervene when a
weight change occurs that may impact the residents' well-being. Further review of the policy revealed the
facility will obtain residents' weights on admission and weekly for four weeks. The nurse and/or dietician will
check the weights and verify if there was a loss or gain of 5% of total weight in one month, or 5 pounds in
one week. A re-weight within 48 hours will be performed to verify actual weight loss. A clinical record review
revealed Resident 15 was admitted to the facility on [DATE], with a diagnosis of a fracture of the lower end
of the right radius (a break in the larger forearm bone near the wrist). A review of an admission Minimum
Data Set assessment (MDS, a federallymandated standardized assessment process conducted at specific
intervals to plan resident care) dated October 29, 2025, revealed the resident was cognitively intact, with a
BIMS (Brief Interview for Mental Status, a tool to assess cognitive function) score of 13 (a score of 13 to 15
indicates cognition is intact). A review of Resident 15's October 23, 2025, weight record revealed that
Resident 15 weighed 151.6 pounds on admission, 150.8 pounds on October 31, 2025, and 144.6 pounds
on November 3, 2025. This represents a seven pound loss since admission and a weight loss of 6.2 pounds
in one week. The clinical record did not contain evidence that the facility completed a reweight within
forty-eight hours as required by facility policy for a weight loss of five pounds in one week. The clinical
record also did not contain evidence that the facility implemented interventions to prevent further weight
loss. There was no documentation of weights or reweighs after November 3, 2025. The surveyor notified the
facility on November 13, 2025, at 10:30 AM that no weights had been documented since November 3,
2025, despite the policy requirement for weekly weights on four occasions after admission. After inquiries
made during the survey, the facility weighed the resident and recorded a weight of 144 pounds. During an
interview with Resident 15 on November 12, 2025, at 11:30 AM, the resident stated she was right hand
dominant and that eating with a cast on her right arm was difficult. The resident stated she was not eating
as much as she normally would at home. During an interview on November 13, 2025, at 1:30 PM, the
Director of Nursing (DON) was unable to provide evidence that the facility timely identified Resident 15's
weight loss and that interventions or discussion of the weight loss to prevent further weight loss was
identified or completed prior to inquiries made during the survey. A clinical record review revealed Resident
22 was admitted to the facility on [DATE], with a diagnosis of a urinary tract infection.A review of the weight
record dated October 27, 2025, revealed an admission weight of 221.8 pounds. A subsequent weight dated
November 2, 2025, revealed a weight of 217.9 pounds. Based on the facility policy, a weekly weight was
required on November 9, 2025. No weight was obtained at that time. The weight was not obtained until
November 13, 2025, at 9:30 AM, after notification by the surveyor, at which time the resident weighed 212.2
pounds. A review of a progress note dated November 13, 2025, at 2:30 PM, revealed that the resident's
meal completion was as low as 26 percent. There was no evidence that the facility obtained Resident 22's
Residents Affected - Some
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395581
If continuation sheet
Page 6 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
weekly weights as required by policy to identify weight loss or initiate appropriate interventions, including
discussion with staff or the resident. During an interview on November 14, 2025, at 10:00 AM, the DON was
unable to provide evidence that the facility's Weighing Residents/Reporting Significant Weight Changes
policy was implemented to timely identify weight loss.A clinical record review revealed that Resident 8 was
admitted to the facility on [DATE], with diagnoses that included status post left above-knee amputation, right
below-knee amputation, diabetes (a condition where the body has too much sugar, known as glucose, in
the blood because it can't effectively use insulin, a hormone that helps glucose get into cells for energy),
and peripheral vascular disease (a slow and progressive circulation disorder caused by narrowing,
blockage, or spasms in a blood vessel). A review of an admission Minimum Data Set assessment (MDS
dated [DATE], revealed the resident was cognitively intact, with a BIMS score of 14, indicating intact
cognition. The resident's care plan initiated September 18, 2025, and revised October 3, 2025, identified
risk factors for weight loss that included decreased appetite, significant weight loss, diabetes, and recent
amputation. The stated goals included maintaining or increasing weight, consuming more than fifty percent
of meals, adhering to a therapeutic diet (meal plan designed to manage or treat a specific medical
condition), and taking prescribed nutritional supplements (a product taken orally to supplement the diet with
extra vitamins, minerals, calories, protein, or other substances to improve nutritional intake). Interventions
planned included providing meal alternatives when meals were refused, administering dietary supplements,
weighing the resident weekly for four weeks and then monthly, and reporting decreased meal intake. A
review of the resident's weight record revealed the following recorded weights: September 18, 2025: 179
pounds (completed three days after admission)September 23, 2025: 172.6 pounds (3.5% weight
loss)October 1, 2025: 164.6 pounds (8% weight loss in 15 days)October 3, 2025: 164.4 pounds (reweight
for October 1, 2025, 8.2% weight loss in 17 days)October 6, 2025: 161.4 poundsOctober 13, 2025: 160.7
poundsOctober 20, 2025: 160.6 poundsNovember 4, 2025: 160.2 pounds (10.5% significant weight loss in
47 days). A review of a nutritional weight warning note dated October 3, 2025, revealed that the resident
had a significant weight loss of 14.2 pounds, which is 8.2 percent, in less than one month The registered
dietitian (RD) recommended Glucerna (a nutritional drink for people with diabetes, which provides extra
calories, protein, and nutrients) once daily to prevent further weight loss. A review of a nutritional weight
warning note dated October 14, 2025, revealed that the resident continued to lose weight, with an
additional loss of 3.7 pounds, which was 2.2 percent, since the October 3, 2025, note. The registered
dietitian discontinued the Glucerna supplement and recommended no sugar added Mighty Shakes (a
nutritional drink without added sugar that provides extra calories, proteins, and nutrients) with meals to
prevent further weight loss. A review of the resident's Task Documentation Record from October 14 through
October 31, 2025, revealed that staff documented the resident consumed between 0 percent and 100
percent of the Glucerna supplement once daily, despite Glucerna being discontinued on October 14, 2025.
Staff also documented consumption of Mighty Shakes three times per day during this same period. A
review of the resident's Task Documentation Record from November 1 through November 13, 2025,
revealed that staff continued to document the resident consumed between 0 percent and 100 percent of the
Glucerna supplement once daily, although the supplement remained discontinued. Staff also documented
the resident consumed between 0 percent and 100 percent of the Mighty Shakes three times per day.
During an interview with Resident 8 on November 13, 2025, at 2:15 PM, the resident stated that he was
aware he had lost weight. The resident stated he did not like the Mighty Shakes because he felt they raised
his blood sugar. The resident stated he preferred Glucerna and reported he had not received Glucerna in
some time. An interview with the foodservice director
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395581
If continuation sheet
Page 7 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
(FSD) on November 13, 2025, at 2:45 PM confirmed that Glucerna was discontinued on October 14, 2025,
and that Mighty Shakes three times per day were initiated by the registered dietitian. The Foodservice
Director was unable to provide documented evidence that the resident's preferences were considered prior
to discontinuing the Glucerna supplement. An interview with the director of nursing (DON) on November 14,
2025, at 9:00 AM confirmed that staff were responsible for accurately documenting on the resident's Task
Documentation Record to accurately reflect what is consumed by a resident. The Director of Nursing
confirmed that Glucerna continued to appear on the resident's October and November Task Documentation
Records despite being discontinued on October 14, 2025. 28 Pa Code 211.5 (f)(ii)(iii)(x) Medical records.
28 Pa. Code 211.10(c) Resident care policies. 28 Pa Code 211.12 (d)(3)(5) Nursing services.
Event ID:
Facility ID:
395581
If continuation sheet
Page 8 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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 0694
Provide for the safe, appropriate administration of IV fluids 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 a
review of clinical records, select facility policy, observations, and staff interviews, it was determined that the
facility failed to provide person-centered care as prescribed to meet the current clinical needs and failed to
follow physician orders for the management of a Peripherally Inserted Central Catheter (PICC) line for three
of 21 sampled residents (Residents 12, 75, and 76). Findings include: A review of the facility policy entitled
Central Venous Catheter/PICC Care/Flush/Medication Administration, last reviewed October 1, 2025,
indicated the facility is to provide dressing changes, medication, and flushes to residents with a PICC line
access (a thin flexible tube that is inserted into a large vein to the heart to deliver medications and other
therapies into the bloodstream) and that all residents with a PICC lines will have emergency care measures
in place in the event of line breakage or dislodgement. Dressing changes are to be made weekly and as
needed with the extension tubing, if applicable, stabilization device, if applicable, and cap change, unless
ordered otherwise by the physician. Further review revealed that the PICC line should be flushed with 10
milliliters (ml) of normal saline prior to medication being administered and after the medication is complete
to flush with 10 ml of normal saline. All residents with a PICC line will have a clamp and dressing kit taped
to the back of their bed's headboard or wall, and placement of these emergency items will be checked
every shift by the designated nurse and documented on the Medication Administration Record (MAR). A
review of clinical records revealed Resident 12 was admitted to the facility on [DATE], with diagnoses to
include osteomyelitis (bone infection) of the lumbar spine and sepsis due to Escherichia coli (E. coli, a
bacterium) and was receiving intravenous (IV, within the vein) antibiotics through a PICC line. A physician
order dated October 12, 2025, directed that an emergency PICC line kit be kept at the bedside and on the
resident's wheelchair and checked every shift. An emergency PICC line kit is a small set of supplies kept
immediately available for residents who have a PICC line. The emergency kit contains a sterile clamp and
dressing materials used to quickly secure the catheter site if the PICC line becomes loose, breaks, leaks, or
is accidentally pulled out. The kit is necessary because a disruption of the PICC line can allow air or
bacteria to enter the bloodstream or cause bleeding. Immediate access to the clamp and dressing allows
staff to stabilize the site until a medical provider can evaluate the resident. Keeping this kit at the bedside or
wheelchair enables staff to respond without delay and reduces the risk of infection, catheter occlusion, loss
of IV access, or other complications. A review of Resident 12's MARs (medication administration record) for
October and November 2025 indicated that nursing staff documented the presence of the emergency PICC
line kit at bedside and on the wheelchair each shift from October 12, 2025, through November 12, 2025.
However, an observation conducted on November 12, 2025, at 11:00 AM, revealed that no emergency
PICC supplies were present at the bedside or on the wheelchair. An interview with Employee 2, Registered
Nurse, on November 12, 2025, at 11:30 AM, confirmed that Resident 12 had a physician's order for
emergency PICC line supplies but that no such supplies were present. A physician order for Resident 12,
dated October 12, 2025, noted an order for ceftriaxone (an antibiotic) 2000 milligrams (mg) intravenous one
time daily for sepsis due to E. coli until November 13, 2025. A physician order for Resident 12, dated
October 12, 2025, noted an order for Sodium Chloride 0.9% flush and to use 10 ml intravenously every shift
to maintain patency. A review of Resident 12's physicians' orders and October and November 2025 MARs
failed to indicate the resident's PICC line was flushed before and after the administration of each IV
antibiotic as per facility policy. A review of clinical records revealed Resident 75 was admitted to the facility
on [DATE], with diagnoses to include sepsis (a medical emergency where the body has
Residents Affected - Some
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395581
If continuation sheet
Page 9 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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 0694
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
an overwhelming inflammatory response to an infection, which can damage tissues and organs) due to
methicillin-susceptible Staphylococcus aureus (MSSA, a type of Staphylococcus aureus that responds to
certain antibiotics), that was present in a left pleural effusion (buildup of excess fluid in the space between
the lungs and chest wall) and was receiving intravenous antibiotics through a PICC line. A review of
physician orders dated November 8, 2025, revealed orders for an emergency PICC line kit to be kept at the
bedside and on the resident's wheelchair and to be checked every shift. A review of Resident 75's
Treatment Administration Record (TAR) for November 2025 indicated that nursing staff documented the
emergency PICC line kit at the bedside and on the wheelchair as present each shift from November 8,
2025, through November 12, 2025. However, an observation conducted on November 12, 2025, at 11:05
AM, revealed no emergency PICC line supplies were available in the resident's room or on the wheelchair.
An interview with Employee 2, Registered Nurse, on November 12, 2025, at 11:30 AM, confirmed that the
emergency supplies were not present despite the physician order.Further review of physician orders dated
November 8, 2025, indicated that the resident's PICC dressing and caps were to be changed weekly on
Saturdays and as needed. Observation of the resident's PICC line dressing on November 14, 2025, at 9:10
AM, in the presence of Employee 1, Registered Nurse, revealed that the dressing was last changed on
November 5, 2025. Employee 1 stated that the dressing should have been changed on November 12,
2025, seven days after the last change. A physician order for Resident 75 dated November 8, 2025,
revealed an order for Cefazolin Sodium (an antibiotic) 2 grams (gm) intravenous every eight hours related
to sepsis until December 9, 2025. A physician order for Resident 75, dated November 8, 2025, noted an
order for Sodium Chloride 0.9% flush and to use 10 ml intravenously every shift to maintain patency. A
review of Resident 75's physicians' orders and the November 2025 MAR failed to indicate the resident's
PICC line was flushed before and after the administration of each IV antibiotic as per facility policy. A review
of the clinical record revealed that Resident 76 was admitted to the facility on [DATE], with diagnoses that
included MSSA after having a right knee replacement surgery on October 7, 2025, and was receiving
intravenous antibiotics through a PICC line. A physician order for Resident 76 dated November 7, 2025,
revealed an order for Cefazolin Sodium (an antibiotic) 2 gm intravenous every eight hours related to wound
infection until December 13, 2025. A physician order for Resident 76, dated November 7, 2025, noted an
order for Sodium Chloride 0.9% flush and to use 10 ml intravenously every shift to maintain patency
(ensuring the line remains open and fluids can be administered without blockage). A review of Resident
76's physicians' orders and the November 2025 MAR failed to indicate the resident's PICC line was flushed
before and after the administration of each IV antibiotic as per facility policy. During an interview with the
Director of Nursing on November 14, 2025, at 11:00 AM the above findings were reviewed and confirmed
regarding Resident 12, Resident 75 and Resident 76's PICC lines. 28 Pa Code 211.10 (a)(c) Resident care
policies.28 Pa. Code 211.12 (c)(d)(1)(3)(5) Nursing services.
Event ID:
Facility ID:
395581
If continuation sheet
Page 10 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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 0697
Provide safe, appropriate pain management for a resident who requires such services.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on a
review of clinical records, select facility policy, controlled substance records, and staff and resident
interviews, it was determined that the facility failed to follow physician orders, complete timely pain
assessments, implement measures to reduce or alleviate pain, reassess the effectiveness of pain
interventions within a reasonable time frame, and accurately document these activities in the clinical record
for three of 21 sampled residents (Residents 15, 45, and 23). Findings include:A review of the facility's
policy entitled Pain Management Process, last reviewed by the facility on October 1, 2025, indicated that
the facility was to ensure resident comfort and that documentation of assessments, interventions, and
outcomes utilized to control pain would be established. Resident pain levels are to be assessed by staff
utilizing a numeric pain scale. Residents who can verbalize their degree of pain would be directed to
provide a numerical number between zero and ten. Zero (0) would indicate no pain. A numeric number
between one and four (1-4) would indicate mild pain. A numeric number between five and seven (5-7)
would indicate moderate pain. A numeric number between eight and ten (8-10) would indicate severe pain.
According to the policy, the physician would be notified of the resident's assessed pain levels, and then
medications for the degree of pain would then be prescribed. The Pain Management Process policy directs
staff to attempt non-pharmacological interventions (non-medication-related interventions to relieve pain
such as repositioning, heat or cold packs, massage and relaxation techniques) prior to administration of
pain medications and to document the results. If non-pharmacological interventions were not successful, a
licensed nurse would then document that a medication was administered and would reassess the resident
to evaluate the effectiveness of the pain relief within a reasonable time frame. A clinical record review
revealed that Resident 15 was admitted to the facility on [DATE], with a diagnosis of a fracture of the lower
end of the right radius (a break in the larger forearm bone near the wrist). A physician's order dated
October 23, 2025, directed staff to administer hydromorphone 2.0 milligrams (an opioid pain-relieving
medication) every four hours as needed for moderate to severe pain. A review of the Individual Resident's
Controlled Substance Record dated October 27, 2025, showed the resident received hydromorphone at
11:40 PM. A review of nursing documentation initiated on October 23, 2025, failed to show documentation
of the resident's pain level at the time of administration, any attempted non-pharmacologic measures prior
to administration, or any reassessment of the resident's pain relief after the medication was provided.
During an interview on November 14, 2025, at 11:00 AM, the Director of Nursing (DON) was unable to
produce evidence that staff implemented the facility's pain management policy for Resident 15. A clinical
record review revealed that Resident 45 was readmitted to the facility on [DATE], with a diagnosis of
fibromyalgia (a chronic condition that causes widespread pain and fatigue) and had recent history of falls .A
review of an admission Minimum Data Set assessment (MDS, a federally mandated standardized
assessment process conducted periodically to plan resident care) dated November 12, 2025, revealed that
Resident 45 was cognitively intact with a BIMS score of 15 (Brief Interview for Mental Status, a tool within
the Cognitive Section of the MDS that is used to assess the resident's attention, orientation, and ability to
register and recall new information; a score of 13-15 indicates cognition is intact). A review of nursing
documentation dated November 11, 2025, at 9:35 PM, revealed that Resident 45 was prescribed
Hydrocodone 10-325 milligrams (an opioid pain-relieving medication) with directions to give one tablet by
mouth every six hours as needed for a moderate pain level of five through seven (5-7) and Hydrocodone
Oral Tablet 10-325 milligrams with directions to give two tablets by mouth every six hours as needed for
severe pain of eight through ten (8-10). A subsequent nurse's note dated
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395581
If continuation sheet
Page 11 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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 0697
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
November 12, 2025, at 1:41 AM documented that at 11:30 PM on November 11, 2025, the resident was
yelling out for pain medication, but staff informed her that the ordered medication was not available in the
facility and would need to be delivered by the pharmacy. Review of the November 2025 controlled
substance record showed that the resident did not receive the medication until 12:36 AM, more than one
hour after staff were notified of her pain, confirming a delay in administration. The Director of Nursing
confirmed on November 13, 2025, at 1:30 PM that the ordered medication was not kept on-site and had to
be obtained from the pharmacy once staff communicated the need. Further review of the clinical record
revealed no documentation that staff notified the physician about the medication's unavailability or
requested alternative pain intervention during the delay. At the time the resident requested pain relief, her
pain was assessed at a level 7 (moderate pain), requiring the administration of one tablet; however, the
controlled substance record showed that two tablets were administered, constituting an incorrect dose.
During an interview on November 14, 2025, at 9:30 AM, the resident confirmed receiving two tablets.
During an interview on November 13, 2025, at 1:30 PM, the Director of Nursing confirmed both the delay
and the incorrect dosage. A clinical record review revealed that Resident 23 was admitted to the facility on
[DATE], with a diagnosis to include osteoarthritis (degenerative joint disease where the cartilage that
cushions the ends of the bones wears down, leading to pain). A physician's order dated November 6, 2025,
revealed that Resident 23 was to be administered Tylenol 650 mg (an over-the-counter pain reliever) as
needed for mild pain. A review of nursing documentation dated November 6, 2025, at 2:15 PM revealed that
Resident 23 requested pain medication for neck discomfort. Further review of the clinical record and the
Medication Administration Record (MAR), dated November 2025, failed to indicate that the resident's pain
level was assessed on the numeric scale, that non-pharmacological interventions were offered, or that pain
medication was administered. A review of Resident 23's care plan dated November 1, 2025, showed that
planned interventions included administering pain medication as ordered and documenting its
effectiveness. During an interview on November 14, 2025, at 11:30 AM, the DON was unable to provide
evidence that Resident 23's pain was fully evaluated or that interventions were timely implemented to
relieve the pain. 28 Pa Code 211.10 (c) Resident care policies. 28 Pa Code 211.12 (d)(3)(5) Nursing
services.
Event ID:
Facility ID:
395581
If continuation sheet
Page 12 of 13
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
395581
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Allied Services Center City Skilled Nursing
80 E. Northampton Street
Wilkes Barre, PA 18701
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
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, review of select facility policy, and staff interviews, it was determined the facility
failed to implement and adhere to procedures to ensure acceptable storage for medications on one of three
nursing units (Nursing Unit 3).Findings include: A review of the facility policy titled Disposition of
Medications: Discontinued Medications, last reviewed by the facility on October 1, 2025, revealed it is the
policy of the facility that under circumstances where medications are discontinued by physician order, a
resident is transferred or discharged and does not take medications with him or her, or in the event of a
resident's death, the medications are marked as discontinued with a label closure. Medications can be
disposed of on-site with a witness and completion of the medication disposition form or returned to the
pharmacy for disposal with that document. The facility policy indicated medications awaiting disposal or
return are stored in a locked secure area designated for that purpose until destroyed or picked up for
destruction by the pharmacy. An observation on November 14, 2025, at 10:21 AM revealed an unsecured
drawer in the Unit 3 Nursing Station. Employee 1, Registered Nurse (RN), indicated that she had no
knowledge of medications stored in that drawer in the nursing station. Employee 1, RN, explained that
medications for disposition should be secured in the medication room and not in a drawer at the nursing
station. The unsecured drawer contained a brown paper bag with the following medications: 3 tablets
Baclofen 10 mg-a muscle relaxer used to reduce muscle spasms.1 tablet Sertraline 50 mg-an
antidepressant used for mood and anxiety.8 tablets Midodrine 25 mg-a medication used to raise low blood
pressure.4 tablets Levetiracetam 250 mg-a seizure-prevention medication.2 tablets Levetiracetam 500
mg-a seizure-prevention medication.3 tablets Atorvastatin 40 mg-a cholesterol-lowering medication.1 tablet
Atorvastatin 80 mg-a cholesterol-lowering medication.1 tablet Ezetimibe 10 mg-a medication used to lower
cholesterol.1 tablet Tamsulosin 0.4 mg- a medication used to improve urination in prostate problems.1
tablet Trazodone 50 mg-a sleep and mood medication.1 tablet Allopurinol 300 mg-a medication used to
prevent gout.1 tablet Plavix (clopidogrel) 75 mg-a blood-thinner used to prevent clots.1 tablet Mirtazapine
7.5 mg-a mood medication that can also help appetite and sleep.1 tablet Thera-M-a daily multivitamin.4
tablets Pantoprazole 40 mg-a medication used to reduce stomach acid and treat reflux.12 tablets Meclizine
25 mg-a medication used to treat dizziness or vertigo.7 tablets Apixaban 2.5 mg -a blood-thinner used to
prevent clots and stroke.1 tablet Apixaban 5 mg-a blood-thinner used to prevent clots and stroke.4 tablets
Atenolol 25 mg-a heart and blood pressure medication.7 tablets Folic acid 1 mg-a vitamin used to treat or
prevent deficiency.1 tablet Donepezil 10 mg-a medication used for memory problems in dementia.1 tablet
Gabapentin 100 mg-a medication used for nerve pain or seizures.1 tablet Memantine 10 mg-a medication
used for memory and thinking problems in dementia.1 tablet Metoprolol 25 mg-a heart and blood pressure
medication.1 Humalog insulin pen-rapid-acting insulin used to lower blood sugar.1 tablet Buspirone 5 mg-a
medication used to treat anxiety. During an interview on November 14, 2025, at 10:35 AM, Employee 2,
RN, indicated that she stored the medications in the Unit 3 nursing station drawer because she left the unit
to attend a meeting. Employee 2, RN, explained that it is facility policy to secure medications for disposition
in the medication storage room. An interview with the Director of Nursing on November 14, 2025, at 11:45
AM confirmed that the facility failed to ensure acceptable storage of medications for disposition, as required
by facility policy. 28 Pa. Code 201.18(b)(1) Management. 28 Pa. Code 211.9(j.1)(3) Pharmacy services. 28
Pa. Code 211.10 (d) Resident care policies. 28 Pa. Code 211.12 (c)(d)(1)(5) Nursing services.
Event ID:
Facility ID:
395581
If continuation sheet
Page 13 of 13