F 0558
Reasonably accommodate the needs and preferences of each resident.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, select facility policy, and resident and staff interviews, it was determined the facility failed to
reasonably accommodate residents' need for call bell accommodation for one out of 29 residents sampled
(Resident 18).Findings include: A review of a facility policy titled Call Light Policy, last reviewed by the
facility on August 7, 2025, revealed that it is the policy to ensure the facility is adequately equipped with a
call light at each resident's bedside, toilet, and bathing facility to allow residents to call for assistance.
Further review revealed that each resident will be evaluated for unique needs and preferences to determine
any special accommodation that may be needed for the resident to utilize the call system, and any special
accommodations will be identified on the resident's person-centered plan of care and provided accordingly,
with examples to include touch pads, larger buttons, and bright colors. A review of Resident 18's clinical
record revealed that the resident was admitted to the facility on [DATE], with diagnoses to include
hemiplegia (paralysis on one side of the body) and muscle wasting and atrophy (thinning of muscle mass).
A review of an admission Minimum Data Set assessment (MDS-a federally mandated standardized
assessment process conducted periodically to plan resident care) dated July 9, 2025, revealed that
Resident 18 had moderately impaired cognition with a BIMS score of 12 (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 8-12 indicates cognition is moderately impaired).
Further clinical record review of a skilled nursing progress note, dated July 17, 2025, revealed that Resident
18 was contracted in both upper and lower extremities. Contractures are a permanent shortening of
muscles, tendons, or joints, often due to immobility or neurological conditions, which can cause stiffness
and limit movement. Observations made during an interview with Resident 18 on August 13, 2025, at
approximately 11:00 AM, revealed that the resident had contractures to both hands. During the interview, it
was revealed that Resident 18 was unable to use his push-button call bell due to these contractures.
Resident 18 stated that he had not been able to use his call bell for assistance at the facility and would like
a touch-sensitive call bell system. An interview with Employee 1, Licensed Practical Nurse, conducted on
August 13, 2025, at approximately 11:15 AM, confirmed the observation that Resident 18 was unable to
utilize the standard push-button call light due to his hand contractures. Following surveyor inquiry,
observation at approximately 12:00 PM on August 13, 2025, revealed that the facility did provide a
touch-sensitive call light device, which Resident 18 was able to operate. During an interview with the
Nursing Home Administrator on August 13, 2025, at approximately 12:30 PM, it was confirmed that
Resident 18 had not been provided with a call system compatible with his physical needs prior to the
surveyor's inquiry. 28 Pa. Code 211.10 (d) Resident care policies. 28 Pa. Code 211.12 (d)(1)(3)(5) Nursing
Services. 28 Pa. Code 201.29 (a) Resident Rights.
Residents Affected - Few
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 14
Event ID:
395288
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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 0627
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Ensure the transfer/discharge meets the resident's needs/preferences and that the resident is prepared for
a safe transfer/discharge.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
clinical record review and staff interview, it was determined the facility failed to demonstrate that a
resident's discharge from the facility was appropriate and necessary, for one of three sampled residents
(Resident 112).Findings include: Clinical record review revealed that Resident 112 was admitted to the
facility on [DATE], with diagnoses to include acute kidney failure (an abrupt decrease in kidney function,
resulting in the retention of waste products) and unsteadiness on feet. Review of an entry Minimum Data
Set Assessment (MDS a federally mandated standardized assessment process completed at specific
intervals to plan resident care) dated July 7, 2025, indicated the resident had a BIMS (brief interview mental
screener that aids in detecting cognitive impairment) score of 14 indicating she was cognitively intact. A
review of Resident 112's hospital discharge history and physical paperwork from July 7, 2025, revealed the
resident had been hospitalized in part due to her inability to care for herself. Review of Resident 112's
clinical record revealed the resident was discharged home from the facility on July 19, 2025. Information
provided from the Area Agency on Aging revealed upon return home the resident had no food in her home
that the only item in the refrigerator/freezer was ice cubes. A review of Resident 112's clinical record
revealed social service notes dated July 18, 2025, indicating residents discharge planning had been
discussed with the resident's family. However, there were no social service notes indicating how the family
would assist the resident with acquiring food and other services to assist the resident in the transition to
home, given the resident's prior difficulty in caring for herself. During an interview on August 14, 2025, at
approximately 11:00 AM, the Director of Social Services (SS) confirmed Resident 112 was to be
discharged to her home. The Director of SS was unable to provide documented evidence that Resident 112
would receive the required care and services to ensure a safe discharge to home. A physician discharge
note dated July 19, 2025, indicated Resident 112 arrived at the facility after a hospitalization due to
increased weakness and inability to care for herself, and was to be discharged home. The facility failed to
demonstrate that the discharge was appropriate. During an interview with the Social Service Director on
August 14, 2025, at 12:00 PM it was unable to provide documented evidence that Resident 112's discharge
was safe and appropriate.28 Pa. Code 201.29(h) Resident rights 28 Pa. Code 201.14(a) Responsibility of
Licensee.
Event ID:
Facility ID:
395288
If continuation sheet
Page 2 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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 0641
Ensure each resident receives an accurate assessment.
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, the Resident Assessment Instrument, and staff interview, it was determined the
facility failed to ensure that Minimum Data Set Assessments accurately reflected the status of two residents
out of 29 sampled. (Residents 21 and 72).Findings include: According to the Resident Assessment
Instrument (RAI) User's Manual (an assessment tool utilized to gather definitive information on a resident's
strengths and needs, which must be addressed in an individualized care plan, and the RAI also assists staff
to evaluate goal achievement and revise care plans accordingly by enabling the facility to track changes in
the resident's status) dated October 2024, Section K0300 Weight Loss the facility is to record loss of 5% or
more in the last month or loss of 10% or more in the last 6 months. A clinical record review revealed
Resident 21 was admitted to the facility on [DATE]. Resident 21 was transferred to the hospital on July 17,
2025, and readmitted to the facility on [DATE]. A review of a Medicare 5 day Minimum Data Set
Assessment (MDS- a federally mandated standardized assessment conducted at specific intervals to plan
resident care) dated July 29, 2025, indicated in Section K0200 that the resident's height was 67 inches and
weight was 107 pounds. Review of Section K0300 indicated that Resident 21 did not experience a weight
loss of 5% or more in the last month or loss of 10% or more in the last 6 months. Review of Resident 21's
Weight Record revealed that on June 13, 2025, the resident weighed 123 pounds. On July 29, 2025, the
resident weighed 107 pounds which is indicative of a 13 % significant weight loss in the last month. During
an interview on August 14, 2025, at approximately 11:00 AM the Registered Dietitian (RD) confirmed that
Resident 21 did experience a 18.6% weight loss between June 13, 2025, and the Medicare 5 day MDS
assessment dated [DATE], and that Section K0300 was inaccurate. According to the RAI User's Manual
dated October 2024, Section O, Special Treatments, Procedures, and Programs O 0110 J1 Dialysis,
indicates facilities will code peritoneal or renal dialysis, which occurs at the nursing home or at another
facility, and record treatments of hemofiltration, slow continuous ultrafiltration (SCUF), continuous
arteriovenous hemofiltration (CAVH), and continuous ambulatory peritoneal dialysis (CAPD) in this item.
Intravenous (IV) medication and blood transfusions administered during dialysis are considered part of the
dialysis procedure. A clinical record review revealed Resident 72 was admitted to the facility on [DATE], with
diagnoses which included end-stage renal disease (final stage of chronic kidney disease in which the
kidneys no longer support the body's needs) with maintenance hemodialysis (a machine filters wastes,
salts, and fluid from the blood when the kidneys are no longer healthy enough to function) every Monday,
Wednesday, and Friday. A review of an admission Minimum Data Set assessment (MDS-a federally
mandated standardized assessment process conducted periodically to plan resident care) Section O 0110.
Special Treatments, Procedures, and Programs, J1, Dialysis completed for Resident 72, dated August 5,
2025, indicated the resident did not receive dialysis treatments while a resident at the facility. Further review
of the clinical record revealed that Resident 72 did receive dialysis treatments on August 1 and August 4,
2025. During an interview on August 13, 2025, at approximately 1:00 PM, the Registered Nurse
Assessment Coordinator (RNAC) confirmed that Resident 72's was receiving dialysis services. The RNAC
confirmed the facility coded Resident 72's MDS assessment dated [DATE], in error as related to dialysis
services. 28 Pa. Code 211.5(f)(i) Medical records. 28 Pa. Code 211.12(d)(3) Nursing services.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395288
If continuation sheet
Page 3 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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 0684
Provide appropriate treatment and care according to orders, resident’s preferences and goals.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
clinical record review, select facility policy, and staff interviews, it was determined the facility failed to
provide professional standards of practice for diabetes management for one resident out of 29 sampled
(Resident 119). Findings include: A review of facility policy entitled Administering Medications, last reviewed
on August 7, 2025, revealed that medications must be administered in accordance with the physician's
orders and if the dosage is believed to be inappropriate or excessive for a resident or a medication has
been identified as having potential adverse consequences for the resident or is suspected of being
associated with adverse consequences, the person preparing or administering the medication shall contact
the resident's attending physician or the facility's medical director to discuss the concerns. A review of
Resident 119's clinical record revealed the resident was admitted to the facility on [DATE], with diagnoses
that included cerebral infarction (brain damage that results from a lack of blood) and diabetes (a chronic
disease that occurs either when the pancreas does not produce enough insulin {a hormone that helps
regulate blood sugar levels} or when the body cannot effectively use the insulin it produces). A review of a
quarterly Minimum Data Set assessment (MDS a federally mandated standardized assessment process
conducted periodically to plan resident care) dated July 22, 2025, revealed that Resident 119 had
moderately impaired cognition with a BIMS score of 9 (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 8-12 indicates cognition is moderately impaired). A clinical
record review for Resident 119 revealed physician orders, dated June 10, 2025, for insulin aspart 5 units
subcutaneous (under the skin) injection four times a day. A review of Resident 119's Medication
Administration Record (MAR) for July 2025 revealed the following:Insulin aspart was held on July 20, 2025,
at 11:00 PM administration with a documented blood glucose of 94 mg/dL.Insulin aspart was held on July
29, 2025, at the 5:00 PM administration with a documented blood glucose of 103 mg/dL.Insulin aspart was
held on July 29, 2025, at the 11:00 PM administration with a documented blood glucose of 118 mg/dL.
Further review of Resident 119's MAR for August 2025 revealed the following:Insulin aspart was held on
August 2, 2025, at the 5:00 PM administration with no blood glucose documented.Insulin aspart was held
on August 2, 2025, at the 11:00 PM administration with a documented blood glucose of 101 mg/dL.Insulin
aspart was held on August 7, 2025, at the 2:00 PM administration with a documented blood glucose of 99
mg/dL. A review of Resident 119's clinical record revealed no physician orders indicating parameters for
holding insulin aspart. Additionally, there was no documented evidence that the physician was notified that
insulin doses had been withheld on the above dates. During an interview with the Nursing Home
Administrator on August 15, 2025, at approximately 10:30 AM, the aforementioned information regarding
the administration of the insulin aspart was reviewed. 28 Pa Code 211.12 (c)(d)(1)(3)(5) Nursing services.
28 Pa Code 211.10 (c)(d) Resident care policies.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395288
If continuation sheet
Page 4 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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, resident observation, and staff interview, it was determined
the facility failed thoroughly assess and timely implement treatments to an identified skin impairment for
one resident out of 29 sampled residents (Resident 16). 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's policy titled Prevention of Pressure Ulcers/Injuries last
reviewed August 7, 2025, indicated staff will inspect the skin on a daily basis and identify any signs of
developing pressure injuries, inspect pressure points such as sacrum (lower back at the base of the spine),
heels, buttocks, coccyx (tailbone), elbows, ischium (lower pelvic bones), and trochanter (hip area).
According to the policy, staff will evaluate, report, and document potential changes in the skin and review
interventions and strategies for effectiveness on an ongoing basis. The policy further states that weekly
body audits will be performed, and a resident-centered care plan will be based upon the risk factors
identified in the assessment. A review of Resident 16's clinical record revealed Resident 16 was admitted to
the facility on [DATE], with diagnoses which included but not limited to Alzheimer's disease, unspecified (a
condition that slowly affects how a person thinks, remembers, and acts) and muscle wasting and atrophy
(muscles become smaller and weaker over time). A review of the March 28, 2025, Minimum Data Set
(MDS-a federally mandated standardized assessment process conducted periodically to plan resident care)
identified Resident 16 required partial/ moderate assistance (helper does less than half the effort) with
aspects of mobility including roll left to side, sitting to lying, sit to stand, chair/bed to chair transfer, and toilet
transfer. Review of the June 20, 2025, MDS noted Resident 16 required substantial/ maximal assistance
(helper does more than half the effort) with aspects of mobility including roll left to side, sitting to lying, sit to
stand, chair/bed to chair transfer, and toilet transfer. The June 20, 2025, MDS illustrated an increase in
assistance and decrease in mobility experienced by Resident 16. Clinical record review of Resident 16's
plan of care that was initiated on February 11, 2024, identified Resident 16 was at risk for pressure ulcer
development related to cognitive deficits and incontinence of bladder and bowel. Among the stated goals
included the absence of skin injury including redness, blisters or discoloration by/through review date.
Planned interventions included administer treatments as ordered and observe for effectiveness as well as
informing MD, responsible party, resident and caregivers of any new area of skin breakdown. A nurse
practitioner progress note dated July 1, 2025, documented a Stage II pressure injury (skin is broken, it's
deeper than red skin but has not gone into the muscle or bone), on the sacral (lower back, base of spine,
tailbone location) area measuring 0.8cm (length) x 0.8cm (width) x 0.1cm (depth), with exposed dermis
(middle layer of skin), no odor, peri wound (skin surrounding wound) was intact, wound base 100%
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395288
If continuation sheet
Page 5 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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
epithelial (covering that lines the skin), light amount of serous exudate (thin, watery drainage), wound
edges were attached, and no pain was evaluated at the time. A treatment was initiated to cleanse with
normal saline, apply Silvasorb gel (a wound dressing with antimicrobial properties) to the base of the
wound, covering with a bordered dressing to be changed daily and as needed. Clinical record review of
Resident 16's ‘Preventative skin care observation' forms for the month of July 2025 and August, 2025
illustrate no new concerns. A review of the Treatment Administration Record (TAR) for July 2025
documented wound treatments were carried out on most days but revealed omissions on July 8, July 9,
July 26, August 1, and August 2, 2025. The clinical record lacked documentation of wound monitoring or
weekly measurements after July 1, 2025. Progress notes by the nurse practitioner from July 8, 2025,
documented refusal of evaluation by the resident but incorrectly indicated the wound was resolved based
only on staff report. Further nurse practitioner notes between July 11 and July 25, 2025, inconsistently
documented that the skin was dry or that no wound care was present, despite the July 1, 2025, diagnosis.
A late entry note on July 31, 2025, by the nurse practitioner, again documented the presence of a sacral
wound. Interview with Director of Nursing (DON), on August 12, 2025, at approximately 12:00 PM, failed to
produce documented evidence that the sacral wound was monitored and confirmed the area had not been
evaluated by the wound consultants since July 1, 2025. The DON confirmed Resident 16 still experienced a
pressure injury in the sacral area. The DON was unable to provide documentation that timely wound care
and pressure injury interventions were initiated to promote healing and monitoring of the Stage II pressure
injury identified July 1, 2025. Following the surveyor inquiry on August 12, 2025, treatment was initiated and
then scheduled to be evaluated by an outside wound consultant. Clinical record review of progress notes
dated August 12, 2025, described an area Moisture Associated Skin Damage (MASD is prolonged
exposure to moisture rather than pressure or friction) and described white slough (dead tissue that
accumulates on the surface of a wound) in the sacral region. The ordered treatment included cleaning the
site with normal saline and applying Silvasorb gel to the area and covering the area with a dressing.
Resident 16 was to be evaluated by the wound consultants the following week according to clinical record
review dated August 12, 2025. On August 14, 2025, at 10:45 AM, surveyor observation of the wound care
by the DON confirmed the presence of a sacral skin injury. Measurements documented that day were 1.5
cm x 1.0 cm x 0 cm, demonstrating enlargement of the wound compared to July 1, 2025. An interview with
the DON on August 14, 2025, at approximately 1:15 PM confirmed the facility could not provide
documented evidence that Resident 16's Stage II sacral, pressure injury was measured and thoroughly
assessed weekly by the staff, wound healing consultants, or the provider. The facility could not provide
documentation, the provider nor the responsible party was informed of the skin injury. 28 Pa. Code
211.10(d) Resident care policies. 28 Pa. Code 211.12(c)(d)(1)(3)(5) Nursing services.
Event ID:
Facility ID:
395288
If continuation sheet
Page 6 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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
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 a
review of facility policy, clinical records, physician orders, resident interview, and staff interview, it was
determined the facility failed to provide restorative nursing services and a therapeutic device prescribed to
maintain mobility and current level of functioning as ordered by the physician and recommended by
rehabilitative therapy staff for one resident (Resident 4) out of five sampled residents. Findings include:
Review of the facility Restorative Nursing Services Policy last updated August 7, 2025, indicated that
residents will receive restorative nursing care as needed to help promote optimal safety and independence.
Residents may be started on a restorative nursing program upon admission, during the course of stay, or
when discharged from rehabilitative care. Restorative goals and objectives are individualized and
resident-centered and are outlined in the resident's plan of care. The resident or resident representative will
be included in determining goals and the plan of care. A review of Resident 4's clinical record revealed that
the resident was admitted to the facility on [DATE], with diagnoses that included hemiplegia (paralysis on
one side of the body) and hemiparesis (weakness on one side of the body) following a cerebral infarction
(stroke) affecting the left non-dominant side. A physical therapy Discharge summary dated [DATE],
recommended a restorative nursing program (RNP) consisting of bilateral lower extremity (BLE) assisted
active range of motion (AAROM) exercises, 10 repetitions times two sets for 15 minutes daily. AAROM is an
exercise in which the resident moves a body part through its range of motion with the assistance of another
person. A physician order dated April 24, 2025, confirmed this recommendation. An occupational therapy
Discharge summary dated [DATE], recommended a restorative nursing program to include active range of
motion (AROM resident moves joints independently without assistance) to the left upper extremity each
joint 10 repetitions times one set. The summary also recommended a splint and brace program, including
inspection of skin integrity, application of a left modified palm guard (a therapeutic device applied to the
hand for individuals with limited hand function) during evening care and removal in the morning, and
positioning the left upper extremity in an elevated and supported position while in bed. Physician orders
dated June 20, 2025, confirmed both the AROM and the splint/brace interventions. A review of Resident 4's
current plan of care identified a focus area of self-care deficit related to stroke, with a goal to improve the
current level of function. However, the plan of care failed to identify or incorporate the resident's restorative
nursing needs as ordered. Interview with Resident 4 on August 15, 2025, at 12:10 PM revealed that he did
not recall receiving any restorative exercises since being discharged from therapy. Resident 4 also noted
that staff have not consistently been applying the palm guard to his left hand. Further review of the clinical
record failed to provide any documented evidence that the resident's restorative nursing was offered to the
resident by staff as ordered by the physician. There was no documented evidence that the resident's
modified palm guard was being applied as ordered by the physician to the resident's left hand. Interview
with the Nursing Home Administrator on August 15, 2025, at approximately 11:30 AM failed to provide
documented evidence that the resident's restorative nursing program which included exercises and a
modified palm guard to the left hand to maintain the resident's mobility to the extent possible were being
provided as ordered by the physician. 28 Pa. Code: 211.5(f)(i)(ii) Medical records. 28 Pa Code 211.1 (d)
Resident care policies. 28 Pa Code 211.12 (c)(d)(5) Nursing services.
Event ID:
Facility ID:
395288
If continuation sheet
Page 7 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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 0689
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Ensure that a nursing home area is free from accident hazards and provides adequate supervision to
prevent accidents.
Based on observations and staff interviews, it was determined that the facility failed to demonstrate an
effective maintenance program of inspection of all bed frames with bed extenders to assure the limiting of
entrapment zones and promote resident safety for two residents out of 29 sampled (Resident 1 and
Resident 7) and in three resident rooms observed.Findings included: Entrapment is a situation in which a
resident's head, neck, chest, or limbs can become trapped between parts of a hospital bed system such as
the mattress, bed frame, side rails, or footboard. The U.S. Food and Drug Administration (FDA) and the
Centers for Medicare & Medicaid Services (CMS) according to Guidance for Industry and FDA Staff:
Hospital Bed System Dimensional and Assessment Guidance to Reduce Entrapment issued March 10,
20026 identify seven potential entrapment zones, including the space between the mattress and the
footboard of the bed (Zone 6). Zone 7 Between the Head or Foot Board and the End of the Mattress When
there is too large of a space between the inside surface of the headboard or footboard and the end of the
mattress, the risk of head entrapment increases. Such gaps can result in serious injury or death if a
resident becomes caught in them. Facilities are expected to inspect and maintain bed systems to minimize
or eliminate entrapment hazards. Observations made during an interview with Resident 7 on August 13,
2025, at approximately 9:00 A.M., revealed a bed frame with a bed extender being utilized due to the
resident's height that had an approximately 4 inches to 6 inch gap from the bottom of the mattress to the
footboard of the bed. Observations made of Resident 1 on August 13, 2025, at approximately 9:30 A.M.,
revealed a bed frame with a bed extender that had a gap from the bottom of the mattress to the footboard
that was filled in with wedges that are normally used for repositioning. Observations made during a tour of
the facility of the second floor on August 13, 2025, at approximately 9:35 A.M., revealed a bed frame with a
bed extender that had a gap from the bottom of the mattress to the footboard in rooms 205-B and 210-B.
An interview on August 15, 2025, at approximately 10:00 A.M., with the physical therapy director, revealed
that when a bed extender is used, it was the facility's practice to place a wedge in the gap created by the
extender. The director acknowledged that wedges commonly used for repositioning were being applied in
these circumstances. The information regarding bed extenders and maintenance of bed gaps was reviewed
with the Nursing Home Administrator on August 15, 2025, at approximately 10:15 A.M. 28 Pa. Code 201.18
(e) (2.1) Management.
Event ID:
Facility ID:
395288
If continuation sheet
Page 8 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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
clinical record review, review of facility policy, and staff interviews, it was determined that the facility failed to
follow its own policies and procedures for monitoring nutritional status, obtaining weights, completing
reweights, and ensuring timely notification of significant weight changes for six of ten sampled residents
(Residents 16, 18, 21, 97, 107, and 119). Findings include: A review of the facility's Nutritional Assessment
Policy last reviewed August 7, 2025, indicated that as part of the comprehensive assessment, a nutritional
assessment, including nutritional status and risk factors for impaired nutrition, shall be conducted for each
resident. The dietitian, in conjunction with the nursing staff and healthcare practitioners, will conduct a
nutritional assessment for each resident upon admission and as indicated by change in condition that place
the resident at risk for impaired nutrition. The nutritional assessment will be conducted by the
interdisciplinary team and identify components which include Nursing: current height and weight, a
description of the resident's usual intake and appetite, a history of reduced appetite or progressive weight
loss or gain prior to admission, a description of the resident's overall appearance, Physician: current clinical
conditions and recent events that may have affected a resident's nutritional status and risk factors, current
laboratory results related to fluid and electrolyte status, and the presence of chewing or swallowing
abnormalities, and Dietitian: an estimate of calorie, protein, and fluid needs, whether the resident's current
intake is adequate to meet his or her nutritional needs, and special food formulations. A review of the facility
Weight Policy last reviewed August 7, 2025, indicated the multidisciplinary team will strive to prevent,
monitor, and intervene for undesirable weight loss for residents. Nursing staff will measure resident weights
on admission and the next day, weekly for four weeks then monthly thereafter. Obtain weights as needed
based on acuity. Weights will be recorded in the resident's medical record. Any weight change of 5% or
more since the last weight assessment will be retaken the next day for confirmation. If the weight is verified,
nursing will immediately notify the dietitian. The dietitian will review individual weight trends over time.
Negative trends will be evaluated by the treatment team whether the criteria for significant weight change
have been met. The threshold for significant unplanned and undesired weight loss will be based on the
following criteria: 1 month 5% weight loss is significant; 3 months 7.5% weight loss is significant; 6 months
10% weight loss is significant. Clinical record review noted Resident 16 was admitted to the facility on
[DATE], with diagnoses which included but not limited to Alzheimer's disease, unspecified (a condition that
slowly affects how a person thinks, remembers, and acts), Muscle wasting and atrophy (muscles become
smaller and weaker over time). Clinical record review of the nutrition notes dated March 11, 2025, reported
a weight of 113 lbs. and confirmed Resident 16 experienced a significant loss of 9.0 lbs. (7.4%) in 30 days,
significant loss of 12.0 lbs. (9.6%) in 90 days, and a non-significant loss of 5.0 lbs. (4.2%) in 180 days.
Ensure (commercially prepared nutritional beverage) was then recommended on March 11, 2025, to
address the weight loss. There was no documented evidence that Resident 16's resident representative
and provider was notified. Further review of the nutrition note, dated April 25, 2025, documented the
resident's weight as 109 pounds and confirmed that the resident continued to experience weight loss of
6.2% in approximately 50 days and 7.5% in 90 days. There was no documented evidence in the clinical
record that further nutritional interventions were initiated at that time, or that the resident's physician or
resident representative was notified of the changes. A progress note dated May 9, 2025, documented a
change in nutritional supplements, discontinuing Ensure (a commercially prepared nutritional beverage)
and substituting double desserts, citing the resident's lack of tolerance and acceptance of Ensure. The
Residents Affected - Some
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395288
If continuation sheet
Page 9 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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
clinical record contained no documented evidence that the resident's weight trend or response to this
intervention was evaluated in accordance with facility policy. Review of the nutrition note, dated June 20,
2025, documented the resident's weight at 108.2 pounds and showed a cumulative weight loss of 16.8
pounds (13.4%) in 180 days. There was no documented evidence that the resident's physician or
representative was notified of this significant weight loss, nor was there evidence that the required reweight
was obtained to confirm accuracy or prompt reassessment of nutritional interventions. Clinical record
review revealed that Resident 18 was admitted to the facility on [DATE], with diagnoses to include
hemiplegia (paralysis on one side of the body) and muscle wasting and atrophy (thinning of muscle mass)
and was dependent on tube feedings for nutrition. The resident was weighed on admission and the
following day; however, no weekly weights were obtained for the next four weeks as required by facility
policy. Records showed that the last documented weight was July 4, 2025, with no further weights until
August 13, 2025, after surveyor inquiry. Resident 18 was weighed on August 13, 2025, and weighed 138
lbs. Interview with the registered dietitian on August 14, 2025, at 10:00 AM confirmed that Resident 18's
weight monitoring was not completed as per facility policy. Clinical record review revealed that Resident 21
was admitted to the facility on [DATE], with diagnoses including dementia (a condition marked by loss of
memory, reasoning, and thinking severe enough to interfere with daily life). On admission, the resident's
weight was documented at 123 pounds.Review of the resident's weight record showed no documented
evidence that weekly weights were obtained for four weeks following admission, as required by the facility's
Weight Policy. Further review of the clinical record revealed that the resident was transferred to the hospital
on July 17, 2025, and readmitted to the facility on [DATE]. A subsequent weight, documented on July 29,
2025 (six days after readmission), showed the resident weighed 107 pounds. This represented a 16-pound
(13%) weight loss since June 13, 2025, which meets the facility's definition of significant weight loss. There
was no documented evidence that a required reweight was obtained to confirm this loss. As of surveyor
review on August 14, 2025, there was no documented evidence that further weights were obtained, despite
the documented weight loss and facility policy requiring weekly weights for four weeks upon admission or
readmission. A dietitian note dated July 24, 2025, recorded the last available weight as 123 pounds and
recommended that nursing staff obtain a current weight. A dietitian weight warning note dated August 1,
2025, documented that the resident may have lost 16 pounds (13%) in approximately 45 days. The note
further indicated the resident was consuming more than 75% of meals and taking Ensure (nutritional
beverage supplement) twice daily with fair acceptance, making it unlikely that the resident had lost such a
large amount of weight in that short period. The note directed staff to obtain a reweight and provide
additional dessert as an intervention. Further review of the clinical record revealed no documented
evidence that the physician or resident representative was notified of the possible weight loss, and no
documented evidence that the recommended reweight was obtained as directed by the dietitian. Review of
findings with the registered dietitian on August 14, 2025, confirmed that Resident 21's weight monitoring
was not carried out according to the facility's Weight Policy. Clinical record review revealed that Resident 97
was admitted to the facility on [DATE], with diagnoses including moderate protein-calorie malnutrition (an
imbalance between the nutrients needed by the body and the nutrients actually consumed). Further review
of the resident's weight record showed that the resident weighed 118 pounds on June 6, 2025, and 110
pounds on July 2, 2025, reflecting an 8 pound loss (6.7%) in 30 days. An unplanned weight loss greater
than 5% in 30 days meets the facility's definition of significant weight loss. A dietitian weight warning note
dated July 3, 2025, acknowledged the 8 pound (6.7%) weight loss in approximately 30 days. The note
further documented that the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395288
If continuation sheet
Page 10 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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
resident was consuming more than 75% of meals with a fair intake of Ensure (a commercially prepared
nutritional beverage) and health shakes twice daily. The dietitian recorded that it was unlikely the resident
had lost such a large amount of weight in that short timeframe and suggested that the June weight was
likely an error. The note recommended continued monitoring of weights and laboratory values. Despite this
recommendation, there was no documented evidence that weekly weights were obtained for four weeks as
required by the facility's Weight Policy. Further review of the clinical record revealed no documented
evidence that the resident's physician or representative was notified of the significant weight loss, as
required by facility policy. Clinical record review revealed that Resident 107 was admitted to the facility on
[DATE], with diagnoses including diabetes and dysphagia (difficulty swallowing). A nutritional assessment
dated [DATE], documented that the resident's hospital weight prior to admission was 157 pounds. The
assessment also recorded a history of significant weight loss of 13 pounds, or 7.6%, in three months as
noted in the hospital record. Review of the resident's weight record revealed that on August 13, 2025,
fourteen days after admission, the resident's weight was documented as 150 pounds. This represented a
continued weight loss. There was no documented evidence that weights were obtained in a timely manner
following admission, as required by the facility's Weight Policy. Review of findings with the registered
dietitian on August 14, 2025, confirmed that Resident 107's weight monitoring was not completed in
accordance with facility policy. Clinical record review revealed that Resident 119 was admitted to the facility
on [DATE], with diagnoses including cerebral infarction (brain damage caused by lack of blood supply to the
brain) and dependence on tube feedings for nutrition. Review of the resident's weight record showed that
on May 16, 2025, the resident weighed 302.4 pounds. A nutrition progress note completed by the
registered dietitian on July 3, 2025, documented the most recent weight as 302.4 pounds, with the note
indicating that the resident's weight reflected stability. There was no documented evidence that monthly
weights were obtained after May 16, 2025, as required by the facility's Weight Policy. A subsequent nutrition
progress note dated July 22, 2025, again documented the most recent weight as 302.4 pounds from May
16, 2025, and reflected stability, despite no monthly weights being documented in the record as required.
The weight record then showed that on July 29, 2025, the resident weighed 257 pounds, representing a
potential 45.4 pound (15.0%) weight loss in approximately 70 days. A nutrition progress note dated August
1, 2025, documented that the July 29, 2025, weight was likely an error and recommended a reweight to
confirm accuracy. The note further directed that, if the weight loss was confirmed, consideration for
nutritional interventions would be assessed. Further review of the clinical record revealed no documented
evidence that a reweight was obtained, as requested by the dietitian. There was also no documented
evidence that the resident's physician or representative was notified of the potential significant weight loss.
Review of findings with the registered dietitian on August 14, 2025, at 10:00 AM, confirmed that Resident
119's weight monitoring was not completed in accordance with facility policy. Review of findings with the
nursing home administrator on August 15, 2025, confirmed that weight monitoring for the above-mentioned
residents had not been consistently completed as required by policy to ensure accurate assessment of
nutritional status and timely planning of nutritional support. 28 Pa Code 211.10 (a)(c) Resident care
policies. 28 Pa Code 211.12 (c)(d)(3)(5) Nursing services.
Event ID:
Facility ID:
395288
If continuation sheet
Page 11 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
Based on a review of controlled drug shift count records, select facility policy, observations of the
medication cart, and staff interviews, it was determined that the facility failed to implement procedures to
promote accurate documentation of controlled medications for one of three medication carts reviewed (first
floor, back cart). Findings include: A review of facility policy entitled Controlled Substances last reviewed on
August 7, 2025, revealed that nursing staff must count controlled medications at the end of each shift. The
policy further stated that the nurse coming on duty and the nurse going off duty must complete the count
together and that both nurses are required to sign the record to verify accuracy. In addition, the policy
directed that any discrepancies must be reported to the Director of Nursing Services immediately A review
of controlled drug records (also known as narcotics are medications that are regulated by federal law due to
their high risk of abuse or misuse) for the first-floor, back medication cart revealed multiple instances in
which the required signatures verifying narcotic counts were missing: January 14, 2025, the off coming
nightshift nurse failed to sign that the narcotic count was completed and correct,January 15, 2025, the
nightshift on coming nurse failed to sign that the narcotic count was completed and correct, and the off
coming night shift nurse failed to sign that the narcotic count was completed and correct,January 17, 2025,
the off going evening nurse failed to sign that the narcotic count was completed and correct, andAugust 10,
2025, the oncoming evening nurse failed to sign that the narcotic count was completed and correct, and off
coming evening nurse failed to sign that the narcotic count was completed and correct. An interview with
Employee 2, licensed practical nurse, on August 14 ,2025, at approximately 9:00 AM, confirmed the
narcotic sheets on the dates listed above were not signed by the oncoming and off-going nurses as
required. The information was reviewed with the Director of Nursing on August 14, 2025, at approximately
10:30 A.M. The review confirmed that the facility had not consistently implemented its established
procedures to ensure accurate documentation of controlled substances. 28 Pa Code 211.12 (c)(d)(1)(3)(5)
Nursing service. 28 Pa Code 211.9 (c)(k) Pharmacy services. 28 Pa Code 211.5 (f)(x) Clinical records. 28
Pa Code 211.10 (c)(d) Resident care policies.
Event ID:
Facility ID:
395288
If continuation sheet
Page 12 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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 - Few
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 facility policy, review of manufacturer instructions, and staff interviews, it
was determined the facility failed to implement and adhere to procedures to ensure acceptable storage and
use-by dates for multi-dose medications on one of three medication carts (first floor, back cart).Findings
include: A review of the facility policy titled Storage of Medications, last reviewed by the facility on August 7,
2025, revealed that the facility shall not use discontinued, outdated, or deteriorated drugs or biologicals and
that all such drugs shall be returned to the dispensing pharmacy or destroyed. A review of manufacturer
instructions for Humalog Kwik Pen, Basaglar Kwik Pen, and Humalog Insulin vials revealed that these
medications must be stored in the refrigerator until ready for use. Once removed from refrigeration, the
insulin vials and pens may be used for up to 28 days. After 28 days, they are to be discarded. On August
14, 2025, at approximately 9:00 A.M., an observation of the first floor, back medication cart was conducted
in the presence of Employee 2, a licensed practical nurse. The cart contained a Humalog KwikPen that had
been opened on July 5, 2025, a Humalog Insulin vial that had been opened on July 5, 2025, and a
Basaglar KwikPen that had been opened on July 11, 2025. These insulin medications were opened and
available for resident use despite being beyond the manufacturer's recommended 28-day discard date. An
interview with Employee 2 at the time of the observation on August 14, 2025, at approximately 9:00 AM,
revealed the above medications were beyond the manufacturer's recommended 28-day discard date, and
the medications should have been removed from the medication cart and discarded. On August 14, 2025,
at approximately 10:30 A.M., the above findings were reviewed with the Director of Nursing. The review
confirmed that the facility had not adhered to manufacturer guidelines and facility policy regarding the
acceptable storage and use-by dates for multi-dose medications. 28 Pa. Code 211.9(a)(1)(k) Pharmacy
services. 28 Pa. Code 211.12(c)(d)(1)(5) Nursing services. 28 Pa Code 211.10 (c)(d) Resident care
policies.
Event ID:
Facility ID:
395288
If continuation sheet
Page 13 of 14
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
395288
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/15/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sapphire Care and Rehab Center
221 East Brown Street
East Stroudsburg, PA 18301
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 0909
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Regularly inspect all bed frames, mattresses, and bed rails (if any) for safety; and all bed rails and
mattresses must attach safely to the bed frame.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation and staff interview, it was determined that the facility failed to ensure the availability of a
functioning bed for all current licensed and certified resident beds on two of three resident care units, (first
floor and second floor).Findings include: The facility is licensed and certified by the State and the Centers
for Medicare & Medicaid Services (CMS) for a specific number of resident beds. The facility must provide
residents with bedrooms that are appropriately furnished with a bed, mattress, and related equipment in
accordance with the facility's license and certification. Licensed capacity, in plain terms, is the maximum
number of residents the facility is legally permitted and expected to be accommodated at any given time.
Beds must be physically present to demonstrate that the facility is able to provide immediate, safe, and
appropriate accommodations for its licensed capacity, and not merely maintain bed space on paper.
Observations made during an environmental tour August 14, 2025, at 11:30 A.M., multiple missing resident
beds were observed on the first and second floor units, as follows: Resident room [ROOM NUMBER],
licensed as a triple room, contained no bed for 104B.Resident room [ROOM NUMBER], licensed as a triple
room, contained no bed for 106B.Resident room [ROOM NUMBER], licensed as a double room, contained
no bed for 113B.Resident room [ROOM NUMBER], licensed as a double room, contained no bed for
116B.Resident room [ROOM NUMBER], licensed as a double room, contained no bed for 217B. These
observations confirmed that the facility did not maintain the full complement of licensed and certified beds,
as several licensed resident spaces were without a functioning bed and mattress. The missing beds were
not stored elsewhere in the facility and therefore were not available for immediate use. A review of the
findings with the Nursing Home Administrator on August 14, 2025, at approximately 12:00 p.m. was
conducted and confirmed. 28 Pa Code 201.18(b)(1) Management. 28 Pa Code 205.20 Resident rooms.
Event ID:
Facility ID:
395288
If continuation sheet
Page 14 of 14