Pennsylvania Department of Health
MEADOWCREST REHABILITATION & HEALTHCARE CENTER
Patient Care Inspection Results

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MEADOWCREST REHABILITATION & HEALTHCARE CENTER
Inspection Results For:

There are  123 surveys for this facility. Please select a date to view the survey results.

Surveys don't appear on this website until at least 41 days have elapsed since the exit date of the survey.
MEADOWCREST REHABILITATION & HEALTHCARE CENTER - Inspection Results Scope of Citation
Number of Residents Affected
By Deficient Practice
Initial comments:Based on a Medicare/Medicaid Recertification survey, State Licensure survey and Civil Rights Compliance survey completed on March 6, 2026, it was determined that Meadowcrest Rehabilitation &; Healthcare was not in compliance with the requirements of 42 CFR Part 483, Subpart B, Requirements for Long Term Care and the 28 Pa. Code, Commonwealth of Pennsylvania Long Term Care Licensure Regulations.
 Plan of Correction:


483.60(a)(1)(2) REQUIREMENT Qualified Dietary Staff:This is a less serious (but not lowest level) deficiency but was found to be widespread throughout the facility and/or has the potential to affect a large portion or all the residents.  This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.60(a) Staffing
The facility must employ sufficient staff with the appropriate competencies and skills sets to carry out the functions of the food and nutrition service, taking into consideration resident assessments, individual plans of care and the number, acuity and diagnoses of the facility's resident population in accordance with the facility assessment required at §483.71.

This includes:
§483.60(a)(1) A qualified dietitian or other clinically qualified nutrition professional either full-time, part-time, or on a consultant basis. A qualified dietitian or other clinically qualified nutrition professional is one who-
(i) Holds a bachelor's or higher degree granted by a regionally accredited college or university in the United States (or an equivalent foreign degree) with completion of the academic requirements of a program in nutrition or dietetics accredited by an appropriate national accreditation organization recognized for this purpose.
(ii) Has completed at least 900 hours of supervised dietetics practice under the supervision of a registered dietitian or nutrition professional.
(iii) Is licensed or certified as a dietitian or nutrition professional by the State in which the services are performed. In a State that does not provide for licensure or certification, the individual will be deemed to have met this requirement if he or she is recognized as a "registered dietitian" by the Commission on Dietetic Registration or its successor organization, or meets the requirements of paragraphs (a)(1)(i) and (ii) of this section.
(iv) For dietitians hired or contracted with prior to November 28, 2016, meets these requirements no later than 5 years after November 28, 2016 or as required by state law.

§483.60(a)(2) If a qualified dietitian or other clinically qualified nutrition professional is not employed full-time, the facility must designate a person to serve as the director of food and nutrition services.
(i) The director of food and nutrition services must at a minimum meet one of the following qualifications-
(A) A certified dietary manager; or
(B) A certified food service manager; or
(C) Has similar national certification for food service management and safety from a national certifying body; or
D) Has an associate's or higher degree in food service management or in hospitality, if the course study includes food service or restaurant management, from an accredited institution of higher learning; or
(E) Has 2 or more years of experience in the position of director of food and nutrition services in a nursing facility setting and has completed a course of study in food safety and management, by no later than October 1, 2023, that includes topics integral to managing dietary operations including, but not limited to, foodborne illness, sanitation procedures, and food purchasing/receiving; and
(ii) In States that have established standards for food service managers or dietary managers, meets State requirements for food service managers or dietary managers, and
(iii) Receives frequently scheduled consultations from a qualified dietitian or other clinically qualified nutrition professional.
Observations: Based on review of employee qualification and staff interview it was determined that the facility failed to employ a qualified Food Service Director to manage the daily operations of the Dietary Department for 12 out of 12 months (April 2025 through March 2026). Findings include: During an interview on 3/4/26, at 9:40 a.m., the Dietary Supervisor stated she was not certified and that the Dietitian only works two days a week. During an interview on 3/4/26, at 10:00 a.m., the Nursing Home Administrator stated that the Registered Dietitian (RD) was not employed full time she comes two times a week. The RD was not on-site full time to oversee the operation of the kitchen in the absence of a full time qualified dietary manager. During an interview on 3/4/26, at 10:12 a.m., the Nursing Home Administrator (NHA) confirmed that the facility failed to provide documented evidence that Dietary Manager Employee E1 met the qualifications for the position of Food Service Director. Pa Code: 201.18(e)(6) Management.
 Plan of Correction - To be completed: 04/14/2026

The residents had no negative outcome for the dietary manager not completing the CDM Course at time of survey. Current Dietary Manager is enrolled in CDM classes. The Dietician will be educated on the requirement of having a CDM in place by the NHA. Until the dietary manager has completed the classes; the Dietician will oversee kitchen staff and complete weekly kitchen audits until the dietary manager is certified. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.80(a)(3) REQUIREMENT Antibiotic Stewardship Program:This is a less serious (but not lowest level) deficiency but was found to be widespread throughout the facility and/or has the potential to affect a large portion or all the residents.  This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.80(a) Infection prevention and control program.
The facility must establish an infection prevention and control program (IPCP) that must include, at a minimum, the following elements:

§483.80(a)(3) An antibiotic stewardship program that includes antibiotic use protocols and a system to monitor antibiotic use.
Observations: Based on review of the facility's infection control policies and procedures and staff interview, it was determined that the facility failed to implement an antibiotic stewardship program for 12 of 12 months (April 2025 -March 2026). Findings include: Review of facility policy "Antibiotic Stewardship Program" last reviewed 1/8/26, with a previous review date of 1/14/25, indicated the Antibiotic Stewardship will focus on monitoring the use of antibiotics, improving antibiotic use by avoiding unnecessary or inappropriate antibiotics. The antibiotic stewardship process will be overseen and managed by the Infection Preventionist who works collaboratively with the medical director, pharmacist, nursing and administrative leadership. Review of the facility's Infection Control surveillance for April 2025- March 2026, failed to include documentation to indicate that antibiotic monitoring was completed. During an interview on 4/6/26, at 12:00 p.m., the Nursing Home Administrator confirmed that the facility failed to implement an antibiotic stewardship program for 12 of 12 months (April 2025-March 2026). 28 Pa. Code: 211.10(c)(d) Resident care policies. 28 Pa. Code: 211.12(d)(1)(2)(3)(5) Nursing services.
 Plan of Correction - To be completed: 04/14/2026

The residents had no negative outcome for the facility not including documentation to indicate that antibiotic monitoring was not completed. Audit conducted on all residents that were on antibiotics by DON for all current residents. DON and IP will educated on requirements of documentation to indicate that antibiotic monitoring was completed by CNO. Audits will be conducted by DON or designee on all new admissions and any change of conditions requiring antibiotics including monitoring and surveillance of infections/antibiotic use for four weeks and then monthly by 2 months. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.

483.80(a)(1)(2)(4)(e)(f) REQUIREMENT Infection Prevention & Control:This is a less serious (but not lowest level) deficiency but was found to be widespread throughout the facility and/or has the potential to affect a large portion or all the residents.  This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.80 Infection Control
The facility must establish and maintain an infection prevention and control program designed to provide a safe, sanitary and comfortable environment and to help prevent the development and transmission of communicable diseases and infections.

§483.80(a) Infection prevention and control program.
The facility must establish an infection prevention and control program (IPCP) that must include, at a minimum, the following elements:

§483.80(a)(1) A system for preventing, identifying, reporting, investigating, and controlling infections and communicable diseases for all residents, staff, volunteers, visitors, and other individuals providing services under a contractual arrangement based upon the facility assessment conducted according to §483.71 and following accepted national standards;

§483.80(a)(2) Written standards, policies, and procedures for the program, which must include, but are not limited to:
(i) A system of surveillance designed to identify possible communicable diseases or
infections before they can spread to other persons in the facility;
(ii) When and to whom possible incidents of communicable disease or infections should be reported;
(iii) Standard and transmission-based precautions to be followed to prevent spread of infections;
(iv)When and how isolation should be used for a resident; including but not limited to:
(A) The type and duration of the isolation, depending upon the infectious agent or organism involved, and
(B) A requirement that the isolation should be the least restrictive possible for the resident under the circumstances.
(v) The circumstances under which the facility must prohibit employees with a communicable disease or infected skin lesions from direct contact with residents or their food, if direct contact will transmit the disease; and
(vi)The hand hygiene procedures to be followed by staff involved in direct resident contact.

§483.80(a)(4) A system for recording incidents identified under the facility's IPCP and the corrective actions taken by the facility.

§483.80(e) Linens.
Personnel must handle, store, process, and transport linens so as to prevent the spread of infection.

§483.80(f) Annual review.
The facility will conduct an annual review of its IPCP and update their program, as necessary.
Observations: Based on a review facility policy, clinical records, observations, and resident and staff interviews, it was determined that the facility failed to ensure an environment free from the spread of infection for five of twelve residents (Residents R1, R4, R6, R12, and R33) and failed to implement an infection control program that included a system of surveillance to identify possible communicable diseases or infections for 12 of 12 months (April 2025 through March 2026). Findings include: Review of the clinical record indicated Resident R4 was admitted on 2/12/25. Review of the facility policy "Enhanced Barrier Precautions" dated 1/8/26, previously dated 1/14/25, indicated, "Enhanced barrier precautions (EHBs) are used as an infection prevention and control intervention to reduce the spread of multi-drug-resistant organisms (MDROs) to residents." "EBPs employ targeted gown and glove use during high contact resident care activities when contact precautions do not otherwise apply. Gloves and gown are applied prior to performing the high contact resident care activity (as opposed to before entering the room).Personal protective equipment (PPE) is changed before caring for another resident.Face protection may be used if there is also a risk of splash or spray." Review of the United States Food and Drug Administration prescribing information indicated, "0.9% Sodium Chloride Irrigation USP is utilized for a variety of clinical indications such as sterile irrigation of body cavities, tissues or wounds, indwelling urethral catheters, surgical drainage tubes, and for washing, rinsing or soaking surgical dressings, instruments and laboratory specimens." The guidance further stated that the sodium chloride solution should be discarded after 24 hours to prevent contamination. Review of Resident R4's Minimum Data Set (MDS-a periodic assessment of care needs) dated 2/19/26, indicated diagnoses of atrial fibrillation (disease of the heart characterized by irregular and often faster heartbeat), diabetes (a metabolic disorder in which the body has high sugar levels for prolonged periods of time), and osteomyelitis (inflammation of bone or bone marrow, usually due to infection). Review of a physician's order dated 2/13/26, indicated that Resident R4's wound vac dressing to be changed three times per week on Monday, Wednesday, and Friday on day shift. Review of a physician's order dated 2/16/26, indicated that Resident R4 was ordered enhanced barrier precautions related to a left foot wound. Review of Resident R4's care plan dated 2/12/26, indicated a plan of care developed for enhanced barrier precautions secondary to surgical wound." During an observation of wound care on 3/4/26, at approximately 3:00 p.m. Licensed Practical Nurse Employee E2 performed wound care without using a gown. Review of current physicians' orders on 3/5/26, revealed seven facility residents to be ordered Enhanced Barrier Precautions (Residents R1, R2, R4, R5, R6, R12, and R33). During an observation of the Fawn and Garden nursing units on 3/5/26, beginning at approximately 11/10 a.m. the room for Residents R1, R4, R6, R12, and R33 did not have signage at the door indicating enhanced barrier precautions. Review of the clinical record indicated Resident R1 was admitted to the facility on 12/3/25. Review of the MDS dated 12/9/25, included diagnoses of paraplegia and neurogenic bladder. Review of Section C: Cognitive Patterns indicated that Resident R1 was cognitively intact. Review of Section M: Skin Conditions indicated the presence of a Stage Four pressure ulcer. Review of the plan of care dated 3/3/26, indicated that Resident R1 had actual skin impairment related to impaired mobility. Included in the interventions was, "Administer treatment per physician order." Review of a physician's order dated 3/3/26, indicated that Resident R1 was to have dressing changes to sacral wound: "Clean with acetic acid 1%, apply zinc oxide to peri wound, apply collagen, calcium alginate and apply ABD bid and prn." During a dressing change observation completed on 3/5/26, at 2:00 p.m. the following was observed: Sterile saline solution was opened and partially used. Resident R1 stated to surveyor, "That shouldn't be opened."A clean barrier was not placed under the wound. Bedding under the wound was soiled with wound drainage.Bath towel used as a clean field on the overbed table. 4x4 gauze placed directly on the bath towel and saturated with normal saline solution. The soiled dressing removed was noted to be dated 3/3/26, without a documented time or staff member who performed the dressing change. Review of facility policy "Infection Control Program" dated 1/8/26, with a previous review date of 1/14/25, indicated the Infection Preventionist will conduct ongoing surveillance of Healthcare Associated Infections (HAI's) and other epidemiologically significant infections that have substantial impact on potential resident outcome and that may require transmission- based precautions and other preventive interventions. Review of the facility's Infection Control documentation for the previous 12 months (April 2025 -March 2026) failed to reveal surveillance for tracking infections for residents for 12 of 12 months (April 2025-March 2026). During an interview on 3/6/26, at approximately 12:00 p.m. the Nursing Home Administrator confirmed the facility failed to ensure an environment free from the spread of infection for five of twelve residents and failed to implement an infection control program that included a system of surveillance to identify possible communicable diseases for April 2025 through March 2026. 28 Pa. Code: 201.14(a) Responsibility of licensee. 28 Pa. Code: 201.18(b)(1)(e)(1) Management. 28 Pa. Code: 211.10(c)(d) Resident care policies. 28 Pa. Code: 211.12(d)(1)(2)(5) Nursing services.
 Plan of Correction - To be completed: 04/14/2026

The residents had no negative outcome for required enhanced barrier precautions not being met. Audit conducted at time of survey was conducted of all residents that required enhanced barrier precautions. All signs were hung and PPE bins outside resident rooms requiring enhanced barrier precautions. All nursing staff were educated on enhanced barrier precautions by CNO. Audits will be conducted by DON or designee on all new admissions and any change of conditions requiring enhanced barrier precautions and staff adhering to wearing PPE per policy for residents in EBP for four weeks and then monthly by 2 months. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.60(i)(1)(2) REQUIREMENT Food Procurement,Store/Prepare/Serve-Sanitary:This is a less serious (but not lowest level) deficiency but was found to be widespread throughout the facility and/or has the potential to affect a large portion or all the residents.  This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.60(i) Food safety requirements.
The facility must -

§483.60(i)(1) - Procure food from sources approved or considered satisfactory by federal, state or local authorities.
(i) This may include food items obtained directly from local producers, subject to applicable State and local laws or regulations.
(ii) This provision does not prohibit or prevent facilities from using produce grown in facility gardens, subject to compliance with applicable safe growing and food-handling practices.
(iii) This provision does not preclude residents from consuming foods not procured by the facility.

§483.60(i)(2) - Store, prepare, distribute and serve food in accordance with professional standards for food service safety.
Observations: Based on a review of facility policy, observations and staff interview it was determined that the facility failed to properly store food products in the Main Kitchen, which created the potential for foodborne illness in one of one deep freezer. Findings Include: Review of the facility policy " Food Receiving and Storage" dated 1/8/26, indicated that all food items will be received and stored in a manner that complies with safe food handling practices. During an observation of the main kitchen on 3/4/26, at 9:40 a.m., revealed food being stored directly under the fans of the deep freezer with ice buildup and approximately three inches from the ceiling of the deep freezer. During an interview on 3/4/26, at 9:43 a.m., the Dietary Supervisor Employee E10 confirmed that the facility failed to properly store food products in the Main Kitchen, which created the potential for foodborne illness. Pa. 28 Code: 211.6(c)(d)(f) Dietary services.
 Plan of Correction - To be completed: 04/14/2026

The residents had no negative outcome for failing to meeting food storage regulations in the deep freezer. All food observed approximately three inches from the ceiling of the deep freezer immediately removed. All kitchen staff educated on proper food storage by Dietician. Audits will be conducted by Dietician or designee weekly by four weeks and monthly by 2 months to ensure food storage requirements are being met. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.10(e)(1),483.12(a)(2),483.45(c)(3)(d)(e) REQUIREMENT Right to be Free from Chemical Restraints:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.10(e) Respect and Dignity.
The resident has a right to be treated with respect and dignity, including:

§483.10(e)(1) The right to be free from any . . . chemical restraints
imposed for purposes of discipline or convenience, and not required to treat the
resident's medical symptoms, consistent with §483.12(a)(2).

§483.12
The resident has the right to be free from abuse, neglect, misappropriation of
resident property, and exploitation as defined in this subpart. This includes but is
not limited to freedom from corporal punishment, involuntary seclusion and any
physical or chemical restraint not required to treat the resident's medical
symptoms.
§483.12(a) The facility must-. . .
§483.12(a)(2) Ensure that the resident is free from . . . chemical restraints
imposed for purposes of discipline or convenience and that are not required to treat the resident's medical symptoms.
. . . .
§483.45(c)(3) A psychotropic drug is any drug that affects brain activities associated with mental processes and behavior. These drugs include, but are not limited to, drugs in the following categories:
(i) Anti-psychotic;
(ii) Anti-depressant;
(iii) Anti-anxiety; and
(iv) Hypnotic.

§483.45(d) Unnecessary drugs-General. Each resident's drug regimen must be free from unnecessary drugs. An unnecessary drug is any drug when used-
(1) In excessive dose (including duplicate drug therapy); or
(2) For excessive duration; or
(3) Without adequate monitoring; or
(4) Without adequate indications for its use; or
(5) In the presence of adverse consequences which indicate the dose should be reduced or discontinued; or
(6) Any combinations of the reasons stated in paragraphs (d)(1) through (5) of this section.

§483.45(e) Psychotropic Drugs. Based on a comprehensive assessment of a resident, the facility must ensure that--

§483.45(e)(1) Residents who have not used psychotropic drugs are not given these drugs unless the medication is necessary to treat a specific condition as diagnosed and documented in the clinical record;

§483.45(e)(2) Residents who use psychotropic drugs receive gradual dose reductions, and behavioral interventions, unless clinically contraindicated, in an effort to discontinue these drugs;

§483.45(e)(3) Residents do not receive psychotropic drugs pursuant to a PRN order unless that medication is necessary to treat a diagnosed specific condition that is documented in the clinical record; and

§483.45(e)(4) PRN orders for psychotropic drugs are limited to 14 days. Except as provided in §483.45(e)(5), if the attending physician or prescribing practitioner believes that it is appropriate for the PRN order to be extended beyond 14 days, he or she should document their rationale in the resident's medical record and indicate the duration for the PRN order.

§483.45(e)(5) PRN orders for anti-psychotic drugs are limited to 14 days and cannot be renewed unless the attending physician or prescribing practitioner evaluates the resident for the appropriateness of that medication.
Observations: Based on review of clinical records, facility policy, and staff interview, it was determined that the facility failed to ensure that resident's medication regime was free from unnecessary psychotropic (substances that act on the brain to alter cognition, perception, and mood) medication for four of seven residents (Resident R22, R4, R7, and R41). Findings include: Review of the facility policy "Psychotropic Medication Use" dated 1/8/26, with a previous review date of 1/14/25, indicated that residents will not receive medications that are not clinically indicated to treat a specific condition. A psychotropic drug is any medication that affects the brain activity associated with mental processes and behavior. PRN orders for psychotropic medications are limited to 14 days unless the physician believes it is appropriate to extend the use with documenting the rationale and evaluated the resident for appropriateness of the medication and includes the duration in the clinical record. Antipsychotic medications will be prescribed at the lowest possible dosage for the shortest period of time and are subject to gradual dose reduction and re-review. Residents will only receive antipsychotic medications when necessary to treat specific conditions for which they are indicated and effective. Review of the clinical record indicated Resident R22 was admitted on 7/1/25. Review of Resident R22's MDS (Minimum Data Set- a periodic review of resident care needs) dated 2/15/26, indicated diagnoses which included head injury from a fall, parkinsonism, lung disease, depression and anxiety. Review of Resident R22's physician order dated 10/23/25, indicated to administer lorazepam (a medication used for short term management of anxiety disorders. It works by enhancing a neurotransmitter to sedate the central nervous system), 1mg tablet every six hours PRN (as necessary) for anxiety. Review of Resident R22's clinical record failed to reveal that the attending physician or prescribing practitioner evaluated the resident for the appropriateness of that medication. Review of the clinical record indicated Resident R4 was admitted on 2/12/25. Review of Resident R4's MDS dated 2/19/26, indicated diagnoses of atrial fibrillation (disease of the heart characterized by irregular and often faster heartbeat), diabetes (a metabolic disorder in which the body has high sugar levels for prolonged periods of time), and osteomyelitis (inflammation of bone or bone marrow, usually due to infection). Further review of the MDS assessment failed to include a psychiatric or neurologic diagnosis. Review of the facility diagnosis list failed to include a psychiatric or neurologic diagnosis. Review of Resident R4's physician order dated 2/13/26, indicated to administer Abilify (Aripiprazole-an antipsychotic medication used to treat serious mental health conditions, including schizophrenia, bipolar I disorder), 5 mg daily. Review of the clinical record indicated Resident R7 was admitted on 3/20/25. Review of Resident R7's MDS dated 12/26/25, indicated diagnoses of dementia (a group of symptoms that affects memory, thinking and interferes with daily life) and muscle weakness. Review of Resident R7's physician order dated 8/12/25, indicated to administer haloperidol (antipsychotic medication used to treat schizophrenia, Tourette's disorder, and severe behavioral problems or acute agitation), 0.5mg every 24 hours PRN (as necessary) for agitation. Review of Resident R7's clinical record failed to reveal that the attending physician or prescribing practitioner evaluated the resident for the appropriateness of that medication. Review of the clinical record indicated Resident R41 was admitted on 11/11/22. Review of Resident R41's MDS dated 2/13/26, indicated diagnoses of dementia and chronic pain. Review of Resident R41's physician order dated 11/25/25, indicated to administer haloperidol 0.5mg every twelve hours PRN for agitation. Review of Resident R41's clinical record failed to reveal that the attending physician or prescribing practitioner evaluated the resident for the appropriateness of that medication. During an interview on 3/6/26, at approximately 10:30 a.m. the Nursing Home Administrator confirmed that the facility failed to ensure that the residents medication regime was free from unnecessary psychotropic medication for four of seven residents. 28 Pa. Code 211.2(d)(3) Medical Director 28 Pa. Code 211.10(a) Resident care policies.
 Plan of Correction - To be completed: 04/14/2026

Resident R 4, 7, 22 and 41 did not experience any adverse effects. The pharmacy sent to the facility their most current recommendations and those recommendations were given to their physician for review. 2. DON/designee to educate licensed staff on orders for psychotropic drugs and usage and to monitor effectiveness or adverse consequences of psychotropic medications and to document monitoring/med effectiveness. 3. DON/designee to conduct house audit on residents on psychotropic meds have the appropriate diagnosis and care plan/documentation regarding med effectiveness. 4. DON/Designee to audit psychotropic drug usage to ensure orders have the appropriate diagnosis and care plan/documentation regarding med effectiveness 5X 1 week, 3x/week for 2 weeks, then monthly x 2 months. 5. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.90(g)(1)(2) REQUIREMENT Resident Call System:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.90(g) Resident Call System
The facility must be adequately equipped to allow residents to call for staff assistance through a communication system which relays the call directly to a staff member or to a centralized staff work area from-

§483.90(g)(1) Each resident's bedside; and
§483.90(g)(2) Toilet and bathing facilities.
Observations: Based on facility observations and staff interview, it was determined that the facility failed to maintain an effective call system for two of five restrooms accessible to residents. Findings include: During an observation on 3/4/26, at approximately 9:38 a.m. the staff restroom on the Garden nursing unit was unlocked. Observation of the restroom revealed no emergency call light or call cord attached for emergency use. During an observation on 3/4/26, at approximately 10:30 a.m. the staff restroom on the Garden nursing unit was unlocked, with the key hanging off the door knob, accessible to residents. Observation of the restroom revealed no emergency call light or call cord attached for emergency use. During an observation on 3/5/26, at approximately 9:45 a.m. the staff restroom on the Fawn nursing unit was unlocked, with the key hanging on a magnetic hook approximately waist height, inside the restroom. Observation of the restroom revealed no emergency call light or call cord attached for emergency use. During an observation on 3/6/26, at approximately 9:30 a.m. the staff restroom on the Fawn nursing unit was unlocked, with the key hanging on a magnetic hook approximately waist height, inside the restroom. Observation of the restroom revealed no emergency call light or call cord attached for emergency use. During an observation on 3/6/26, at approximately 11:30 a.m. the staff restroom on the Garden nursing unit was unlocked, with the key hanging off the door knob, accessible to residents. Observation of the restroom revealed no emergency call light or call cord attached for emergency use. During an interview on 3/6/26, at approximately 10:28 a.m. the Nursing Home Administrator confirmed the facility failed to maintain an effective call system for two of five restrooms accessible to residents. 28 Pa. Code 201.14 (a) Responsibility of licensee 28 Pa. Code 201.18 (b) (1) Management
 Plan of Correction - To be completed: 04/14/2026

The residents had no negative outcome for not maintaining an effective call bell system for staff bathrooms. Bathrooms were immediately locked. Keys were hung on magnetic hook out of reach of residents. All staff educated to maintain the staff bathroom key out of the reach of residents due to lack of call system in the staff bathrooms for residents. by NHA. Audits will be conducted by Administrator or designee weekly by four weeks and monthly by 2 months to ensure an staff bathrooms remain locked and inaccessible to residents. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.80(d)(1)(2) REQUIREMENT Influenza and Pneumococcal Immunizations:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.80(d) Influenza and pneumococcal immunizations
§483.80(d)(1) Influenza. The facility must develop policies and procedures to ensure that-
(i) Before offering the influenza immunization, each resident or the resident's representative receives education regarding the benefits and potential side effects of the immunization;
(ii) Each resident is offered an influenza immunization October 1 through March 31 annually, unless the immunization is medically contraindicated or the resident has already been immunized during this time period;
(iii) The resident or the resident's representative has the opportunity to refuse immunization; and
(iv)The resident's medical record includes documentation that indicates, at a minimum, the following:
(A) That the resident or resident's representative was provided education regarding the benefits and potential side effects of influenza immunization; and
(B) That the resident either received the influenza immunization or did not receive the influenza immunization due to medical contraindications or refusal.

§483.80(d)(2) Pneumococcal disease. The facility must develop policies and procedures to ensure that-
(i) Before offering the pneumococcal immunization, each resident or the resident's representative receives education regarding the benefits and potential side effects of the immunization;
(ii) Each resident is offered a pneumococcal immunization, unless the immunization is medically contraindicated or the resident has already been immunized;
(iii) The resident or the resident's representative has the opportunity to refuse immunization; and
(iv)The resident's medical record includes documentation that indicates, at a minimum, the following:
(A) That the resident or resident's representative was provided education regarding the benefits and potential side effects of pneumococcal immunization; and
(B) That the resident either received the pneumococcal immunization or did not receive the pneumococcal immunization due to medical contraindication or refusal.
Observations: Based on facility policy review, clinical record review, and staff interview, it was determined that the facility failed to offer pneumococcal disease vaccines in accordance with facility policy to seven of nine residents whose vaccines were reviewed. (Residents R5, R8, R14, R16, R12, R7 and R31). Findings include: Review of the facility policy "Pneumococcal Vaccine" dated 1/8/26 with a previous review date of 1/14/25, indicated that all residents are offered the pneumonia vaccine to aid in the prevention of pneumococcal pneumonia upon admission resident are assess for eligibility and when indicated will be offered the vaccine within 30 days of admission. Review of the clinical record indicated that Resident R5 was admitted to the facility on 10/19/25. Review of Resident R5's immunization documentation record did not include that the Pneumococcal vaccine was offered since admission. Review of the clinical record indicated that Resident R8 was admitted to the facility on 1/24/24. Review of Resident R8's immunization documentation record did not include that the Pneumococcal vaccine was offered since admission. Review of the clinical record indicated that Resident R14 was admitted to the facility on 10/7/24. Review of Resident R14's immunization documentation record did not include that the Pneumococcal vaccine was offered since admission. Review of the clinical record indicated that Resident R16 was admitted to the facility on 10/25/25. Review of Resident R16's immunization documentation record did not include that the Pneumococcal vaccine was offered since admission. Review of the clinical record indicated that Resident R12 was admitted to the facility on 12/21/25. Review of Resident R12's immunization documentation record did not include that the Pneumococcal vaccine was offered since admission. Review of the clinical record indicated that Resident R7 was admitted to the facility on 3/20/25. Review of Resident R7's immunization documentation record did not include that the Pneumococcal vaccine was offered since admission. Review of the clinical record indicated that Resident R31 was admitted to the facility on 12/4/21. Review of Resident R31's immunization documentation record did not include that the Pneumococcal vaccine was offered since admission. The last Pneumococcal vaccine had been given in 2013, according to the medical record. During an interview on 3/6/26, at 2:10 p.m., the Nursing Home Administrator confirmed that the facility failed to offer pneumococcal disease vaccines in accordance with facility policy to seven of nine residents whose vaccines were reviewed. (Residents R5, R8, R14, R16, R12, R7 and R31).
 Plan of Correction - To be completed: 04/14/2026

The residents had no negative outcome for failing to offer the pneumococcal vaccine annually after admission. An audit was conducted for all residents who have not been offered the pneumococcal vaccine since admitting to the facility. All residents were offered the pneumococcal vaccine who had not been offered since admitting to the facility. Nursing Staff will be educated on offering the pneumococcal vaccine annually after admission by CNO. DON or designee will audit to ensure all residents are offered the pneumococcal vaccine after admission on annual bases. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.20(f)(5),483.70(h)(1)-(5) REQUIREMENT Resident Records - Identifiable Information:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.20(f)(5) Resident-identifiable information.
(i) A facility may not release information that is resident-identifiable to the public.
(ii) The facility may release information that is resident-identifiable to an agent only in accordance with a contract under which the agent agrees not to use or disclose the information except to the extent the facility itself is permitted to do so.

§483.70(h) Medical records.
§483.70(h)(1) In accordance with accepted professional standards and practices, the facility must maintain medical records on each resident that are-
(i) Complete;
(ii) Accurately documented;
(iii) Readily accessible; and
(iv) Systematically organized

§483.70(h)(2) The facility must keep confidential all information contained in the resident's records,
regardless of the form or storage method of the records, except when release is-
(i) To the individual, or their resident representative where permitted by applicable law;
(ii) Required by Law;
(iii) For treatment, payment, or health care operations, as permitted by and in compliance with 45 CFR 164.506;
(iv) For public health activities, reporting of abuse, neglect, or domestic violence, health oversight activities, judicial and administrative proceedings, law enforcement purposes, organ donation purposes, research purposes, or to coroners, medical examiners, funeral directors, and to avert a serious threat to health or safety as permitted by and in compliance with 45 CFR 164.512.

§483.70(h)(3) The facility must safeguard medical record information against loss, destruction, or unauthorized use.

§483.70(h)(4) Medical records must be retained for-
(i) The period of time required by State law; or
(ii) Five years from the date of discharge when there is no requirement in State law; or
(iii) For a minor, 3 years after a resident reaches legal age under State law.

§483.70(h)(5) The medical record must contain-
(i) Sufficient information to identify the resident;
(ii) A record of the resident's assessments;
(iii) The comprehensive plan of care and services provided;
(iv) The results of any preadmission screening and resident review evaluations and determinations conducted by the State;
(v) Physician's, nurse's, and other licensed professional's progress notes; and
(vi) Laboratory, radiology and other diagnostic services reports as required under §483.50.
Observations: Based on the review of facility policy, observations, clinical records, and staff interviews, it was determined that the facility failed to appropriately document treatments for two of four residents (Residents R4 and R1). Findings include: Review of the facility policy, "Charting and Documentation" dated 1/8/26, previously dated 1/14/25, indicated "All services provided to the resident, progress toward the care plan goals, or any changes in the resident's medical, physical, functional or psychosocial condition, shall be documented in the resident's medical record. The medical record should facilitate communication between the interdisciplinary team regarding the resident's condition and response to care." Review of the facility policy, "Dressings, Dry/Clean" dated 1/8/26, previously dated 1/14/25, indicated for staff to document that date and time the dressing was changed. Review of the clinical record indicated Resident R4 was admitted to the facility on 2/12/25. Review of the Minimum Data Set (MDS - periodic assessment of resident care needs dated 2/19/26, included diagnoses of atrial fibrillation (disease of the heart characterized by irregular and often faster heartbeat), diabetes (a metabolic disorder in which the body has high sugar levels for prolonged periods of time), and osteomyelitis (inflammation of bone or bone marrow, usually due to infection). Review of the plan of care dated 2/13/26, indicated that Resident R4 had actual skin impairment related to an incision and drainage/osteomyelitis. Included in the interventions was, "Wound vac dressing changes three times per week on M-W-F (Monday, Wednesday, Friday)." Review of a physician's order dated 2/13/26, indicated that Resident R4's wound vac dressing to be changed three times per week on Monday, Wednesday, and Friday on day shift. During an interview on 3/4/26, at 2:45 p.m. Licensed Practical Nurse (LPN) Employee E2 stated Resident R4 had not had his wound vac dressing change completed yet that day. Review of Resident R4's Treatment Administration Record (TAR) for March 2026, on 3/4/26, at 2:50 p.m. revealed that LPN Employee E2 had documented that she had completed the wound vac dressing change. During an interview on 3/4/26, at 2:55 p.m. when asked to confirm if Resident R4's wound vac dressing change had been completed as she had stated it was not done, but had documented that it was done, LPN Employee E2 stated that LPN Employee E3 had completed the dressing change. During an interview on 3/4/26, at 3:02 p.m. LPN Employee E3 stated she had not completed Resident R4's dressing change. Review of the clinical record indicated Resident R1 was admitted to the facility on 12/3/25. Review of the MDS dated 12/9/25, included diagnoses of paraplegia and neurogenic bladder. Review of Section C: Cognitive Patterns indicated that Resident R1 was cognitively intact. Review of the plan of care dated 3/3/26, indicated that Resident R1 had actual skin impairment related to impaired mobility. Included in the interventions was, "Administer treatment per physician order.". Review of a physician's order dated 3/3/26, indicated that Resident R1 was to have dressing changes to sacral wound: "Clean with acetic acid 1%, apply zinc oxide to peri wound, apply collagen, calcium alginate and apply abd (medical dressing) bid (twice daily) and prn (as needed)." During a dressing change observation completed on 3/5/26, at 2:00 p.m. the soiled dressing removed was noted to be dated 3/3/26, without a documented time or staff member who performed the dressing change. During an interview, completed during the observed dressing change, on 3/5/26, at approximately 2:10 LPN Employee E4 stated that Resident R4's dressing change was to be completed once daily. At this time, Resident R4 responded to LPN Employee E4's comment and stated that he had not had twice daily dressing changes, "in a very long time." Review of Resident R4's Treatment Administration Record (TAR) for March 2026, on 3/5/26, at 2:25 p.m. confirmed that Resident R4 was to receive twice daily dressing changes and confirmed that LPN Employee E2 had documented that she completed both the morning and evening dressing changes on 3/4/26. During an interview on 3/5/26, at 2:30 p.m. the Nursing Home Administrator and the Director of Nursing were informed that the dressing removed from Resident R4 during the dressing change observation on 3/5/26, was dated 3/3/26, and that incorrect information was entered on the TAR documenting that dressing changes were completed by LPN Employee E2 on 3/4/26, for both the day and evening dressing change. During an interview on 3/6/26, at approximately 12:00 p.m. the Nursing Home Administrator and the Director of Nursing confirmed the facility failed to appropriately document treatments for two of four residents. 28 Pa. Code: 211.5(f)(g)(h) Clinical records.
 Plan of Correction - To be completed: 04/14/2026

Resident R1 and R4 immediately had their dressing changed. Employee E2 was educated and suspended pending investigation, and an ERS was submitted to the Department of health. No other residents were identified from this deficient practice. An audit was completed at time of survey of all current residents with dressing change orders to make sure they were completed an dated appropriately. Licensed nurses educated on the facility wound care policy and completing the dressing changes as ordered and not signing off until dressing is completed by CNO. The DON/designee will complete audits 3 times a weeks for 2 weeks and monthly times 2 months to ensure wound dressings are changed and dated per physicians orders. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.45(c)(1)(2)(4)(5) REQUIREMENT Drug Regimen Review, Report Irregular, Act On:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.45(c) Drug Regimen Review.
§483.45(c)(1) The drug regimen of each resident must be reviewed at least once a month by a licensed pharmacist.

§483.45(c)(2) This review must include a review of the resident's medical chart.

§483.45(c)(4) The pharmacist must report any irregularities to the attending physician and the facility's medical director and director of nursing, and these reports must be acted upon.
(i) Irregularities include, but are not limited to, any drug that meets the criteria set forth in paragraph (d) of this section for an unnecessary drug.
(ii) Any irregularities noted by the pharmacist during this review must be documented on a separate, written report that is sent to the attending physician and the facility's medical director and director of nursing and lists, at a minimum, the resident's name, the relevant drug, and the irregularity the pharmacist identified.
(iii) The attending physician must document in the resident's medical record that the identified irregularity has been reviewed and what, if any, action has been taken to address it. If there is to be no change in the medication, the attending physician should document his or her rationale in the resident's medical record.

§483.45(c)(5) The facility must develop and maintain policies and procedures for the monthly drug regimen review that include, but are not limited to, time frames for the different steps in the process and steps the pharmacist must take when he or she identifies an irregularity that requires urgent action to protect the resident.
Observations: Based on review of clinical records and staff interview, it was determined that the facility failed to provide documentation of medication regimen reviews (MRR) completed at least monthly for three of seven residents (Resident R7, R41 and R22). Findings include: On 3/5/26, the MRRs for Residents R7, R41 and R22 were requested, for the months of September 2025, through February 2026. During an interview on 3/6/26, at approximately 10:30 a.m. the Nursing Home Administrator confirmed that the facility was unable to locate the MRRs for Residents R7, R41 and R22. During an interview on 3/6/26, at approximately 12:00 p.m. the Nursing Home Administrator confirmed that the facility failed to provide documentation of medication regimen reviews completed at least monthly for three of seven residents. 28 Pa. Code: 201.14 (a) Responsibility of licensee. 28 Pa. Code 211.5(f) Medical records. 28 Pa. Code: 211.12(d)(1)(3)(5) Nursing services.
 Plan of Correction - To be completed: 04/14/2026

The Residents .R7, R41, and R22 suffered no ill effects from the MRR not being signed by the medical director. Those cited residents will receive MMR signed by medical director. NHA, or designee, will in-service the DON on the facility "Medication Regimen Review" policy and procedure to ensure that all resident MRR's are addressed in accordance with this policy. The DON, or designee, will audit all current residents MRR's to ensure that they have been addressed properly and in accordance with the facility policy and procedure for the Medication Regimen Review. 4.DON, or designee, will monitor all new MRR's to ensure they are completed timely and accurately in line with the "Medication Regimen Review" policy monthly times 2 months. (MRR's are issued monthly from pharmacy). Results of the audits will be reviewed at the Quality Assurance meetings until substantial compliance has been met.
483.25(d)(1)(2) REQUIREMENT Free of Accident Hazards/Supervision/Devices:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.25(d) Accidents.
The facility must ensure that -
§483.25(d)(1) The resident environment remains as free of accident hazards as is possible; and

§483.25(d)(2)Each resident receives adequate supervision and assistance devices to prevent accidents.
Observations: Based on review of facility policy, clinical record and staff interviews, it was determined that the facility failed to make certain each resident received adequate supervision and assistance to prevent accidents for one of two residents (Resident R8). Findings include: Review of the facility policy "Accidents and Incidents- Investigating and Reporting" dared 1/8/26, with a previous review date of 1/14/25, indicated that all accidents and incidents involving residents, employees, etc., occurring on the premises shall be investigated and reported to the Administrator. The Nurse Supervisor shall promptly initiate and document the investigation of the accident or incident. Incident/Accident reports will be reviewed by the Safety Committee for trends related to the accident and analyze any individual resident vulnerabilities. Review of the clinical record indicated Resident R8 was admitted to the facility on 1/25/24. Review Resident R8's Minimum Data Set (MDS - periodic assessment of resident care needs) dated 2/14/26, indicated diagnoses of dementia, psychotic and mood disturbances, anxiety, obesity and dysphagia. Review of Resident R8's MDS completed on 12/21/25. Review of Section GG Functional Abilities Section 0170 question Mobility rolling left to right indicated that Resident R8 is "02" substantial/maximal assistance for rolling left to right in bed for care. Review of Resident R8's Documentation Survey Report V2(report that is produced from the Nurse Aide documented actual care provided and used when completing Section GG on the MDS) dated January 2026, identified Resident R8 as "01" Dependent for bed mobility rolling left to right for care. During a clinical record review, a progress note dated 1/7/26, indicated Resident R8 had a fall out of bed when being provided care which resulted in a laceration above her eyebrow which required treatment. Review of Resident R8's plan of care for "Falls" indicated resident is at risk for falls and to provide assistance as required. Bilateral fall mats to be in place. During an observation on 3/4/26, at 3:00 p.m., fall mat on right side of bed close to wall and leaning onto wall, no mat on left side of bed and Resident R8 had legs bent leaning towards left side of bed. During an observation on 3/5/26, at 9:00 a.m., fall mat on right side of bed unmoved from previous day and no mat on left side of bed. During an interview on 3/4/25, at 3:00 p.m., Registered Nurse Employee E6 and Nurse Aide (NA) Employee E7 stated that substantial/ maximal assistance requires two staff. During an interview on 3/5/26, at 9:00 a.m., NA Employee E8 stated that substantial/maximal assistance requires two staff. During an interview on 3/5/26, at 10:58 a.m., Therapy Manager Employee E9 stated that Resident R8 was not on caseload since 10/9/25, due to her inability to understand and follow commands and that care was identified to require two staff at all times due to her dementia progression. During an interview on 3/5/26, at 10:28 a.m., the Nursing Home Administrator confirmed that the facility failed to make certain each resident received adequate supervision and assistance to prevent accidents for one of two residents (Resident R8). 28 Pa. Code 201.18(e)(1) Management. 28 Pa. Code 201.29(a)(c)(d) Resident rights.
 Plan of Correction - To be completed: 04/14/2026

Resident R8, Care plan, and Kardex, updated to reflect a two person assist for bed mobility completed for the resident. A review of current residents reviewed to ensure level of assistance for bed mobility is correct on the Kardex and care plan is in place. DON or designee will educate Nursing staff including CNAs on following level of assistance needed per the Kardex/care plan. The DON/Designee will audit five times a week for two weeks and then monthly times two months to ensure the correct level of care for residents is being followed. The results of these audits will be reported to the Facility's Monthly QAPI meeting until compliance is met
483.25(b)(1)(i)(ii) REQUIREMENT Treatment/Svcs to Prevent/Heal Pressure Ulcer:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.25(b) Skin Integrity
§483.25(b)(1) Pressure ulcers.
Based on the comprehensive assessment of a resident, the facility must ensure that-
(i) A resident receives care, consistent with professional standards of practice, to prevent pressure ulcers and does not develop pressure ulcers unless the individual's clinical condition demonstrates that they were unavoidable; and
(ii) A resident with pressure ulcers receives necessary treatment and services, consistent with professional standards of practice, to promote healing, prevent infection and prevent new ulcers from developing.
Observations: Based on the review of facility policy, observations, clinical records, and staff interviews, it was determined that the facility failed to make certain residents were provided necessary treatments and services, consistent with professional standards of practice, for a pressure ulcer (PU/PI - injuries to the skin and underlying tissues resulting from prolonged pressure on the skin) for one of three residents (Resident R1). Findings include: Review of the facility policy, "Prevention of Pressure Ulcers/Injuries" dated 1/8/26, previously dated 1/14/25, indicated the facility will identify pressure ulcer risk factors and interventions for specific risk factors. Review of the facility policy, "Dressings, Dry/Clean" dated 1/8/26, previously dated 1/14/25, indicated for staff to document that date and time the dressing was changed. Review of the clinical record indicated Resident R1 was admitted to the facility on 12/3/25. Review of the Minimum Data Set (MDS - periodic assessment of care needs) dated 12/9/25, included diagnoses of paraplegia (paralysis of the legs and lower body, typically caused by spinal injury or disease) and neurogenic bladder (bladder problems due to disease or injury of the nervous system involved in the control of urination). Review of Section C: Cognitive Patterns indicated that Resident R1 was cognitively intact. Review of Section M: Skin Conditions indicated the presence of a Stage Four pressure ulcer (Full-thickness skin and tissue loss). Review of the plan of care dated 3/3/26, indicated that Resident R1 had actual skin impairment related to impaired mobility. Included in the interventions was, "Administer treatment per physician order." Review of a physician's order dated 3/3/26, indicated that Resident R1 was to have dressing changes to sacral wound: "Clean with acetic acid 1%, apply zinc oxide to peri wound, apply collagen, calcium alginate and apply abd (medical dressing) bid (twice daily) and prn (as needed)." During a dressing change observation completed on 3/5/26, at 2:00 p.m. the following was observed: The soiled dressing removed was noted to be dated 3/3/26, without a documented time or staff member who performed the dressing change. LPN Employee E4 used normal saline solution to clean Resident R4's wound. LPN Employee E3 suggested the use of soap and water to clean Resident R4's wound. LPN Employee E4 stated that Resident R4's dressing change was to be completed once daily. Resident R4 responded to LPN Employee E4's comment and stated that he had not had twice daily dressing changes, "in a very long time." Review of Resident R4's Treatment Administration Record (TAR) for March 2026, on 3/5/26, at 2:25 p.m. confirmed that Resident R4 was to receive twice daily dressing changes and confirmed that LPN Employee E2 had documented that she completed both the morning and evening dressing changes on 3/4/26. During an interview on 3/5/26, at 2:30 p.m. the Nursing Home Administrator and the Director of Nursing were informed that the dressing removed from Resident R4 during the dressing change observation on 3/5/26, was dated 3/3/26, and that incorrect information was entered on the TAR documenting that dressing changes were completed by LPN Employee E2 on 3/4/26, for both day and evening dressing change. During an interview on 3/6/26, at approximately 12:00 p.m. the Nursing Home Administrator and the Director of Nursing confirmed the facility failed to make certain residents were provided necessary treatments and services, consistent with professional standards of practice, for a pressure ulcer for one of three residents. 28 Pa. Code: 211.12(d)(5) Nursing Services.
 Plan of Correction - To be completed: 04/14/2026

During survey Resident R4, and R1 was assessed, and order validated that current order in place for treatment of pressure ulcer is correct. 2. Facility residents with current wounds were audited to ensure appropriate and current order in place for treatment of wound and dressings are changed as ordered/correct time interval. 3. Don, or designee will educate licensed staff on wound treatment and following physicians orders policy for admissions and re-admissions. 4. DON, or designee will conduct an audit for admissions and re-admissions to ensure that treatment orders are being followed, and dressing change/assessments are being completed per physicians orders weekly/dressing changes to ensure they are done at the ordered interval and per physician order needs x 2 weeks, then monthly times 2 months. 5.Results of the audits will be reviewed at the Quality Assurance meetings until substantial compliance has been met
483.25 REQUIREMENT Quality of Care:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§ 483.25 Quality of care
Quality of care is a fundamental principle that applies to all treatment and care provided to facility residents. Based on the comprehensive assessment of a resident, the facility must ensure that residents receive treatment and care in accordance with professional standards of practice, the comprehensive person-centered care plan, and the residents' choices.
Observations: Based on resident interview, observations, clinical record review, and staff interviews, it was determined that the facility failed to provide care and services needed for residents to attain or maintain the highest practicable physical, mental, and psychosocial well-being for one of two residents (Resident R26). Findings include: During an interview on 3/4/26, at 8:54 a.m., Resident R26 stated that she has itchiness around the abdomen due to the facility not providing "latex free: incontinence pads prior to the night nurse finding her a latex free brief which does not fit properly and that she has not gotten her eye drops that the doctor ordered a "couple days ago". Resident R26's daughter was on the phone with her and stated that she has a latex allergy, and the doctor told her the eye drops would help her because the resident has dry eyes. During an observation there was a tan colored brief laying on the windowsill, and a package of size large briefs had been opened and Resident R26 showed that it was too small for her. Resident R26's left eye appeared reddened. During an observation of the Fawn nursing unit medication cart, Resident R26 did not have eye drops identified in the cart. During a review a latex allergy was indicated on Resident R26's clinical record and an order for Artificial Tears 2 drops both eyes twice per day and 1 drop both eyes every 6 hours as needed. During an interview on 3/4/26, at 11:08a.m., Registered Nurse Employee E5 stated she did not know why the eye drops had been documented as given and were not available. During an interview on 3/4/26, at 11:48 a.m., the Nursing Home Administrator confirmed that the facility failed to provide care and services needed for residents to attain or maintain the highest practicable physical, mental, and psychosocial well-being for one of two residents (Resident R26). 28 Pa. Code 201.18 (b)(1) Management 28 Pa. Code 201.29(d) Resident Rights 28 Pa. Code 211.10 (c)(d) Resident Care policies 28 Pa. Code 211.12 (d)(1)(2)(3)(5) Nursing services
 Plan of Correction - To be completed: 04/14/2026

During annual survey the facility reviewed resident R 26 use of latex free briefs due to allergy. The facility was able to show that the facility only uses and had in stock latex free briefs. It was determined that the brief the resident had used non latex free briefs while she was in the hospital. The eye drops were stat ordered for the resident and received the same day and were given to the resident. The DON completed a whole house audit and found no other residents had briefs with latex / and no other residents medications listed as unavailable. The DON/designee to educate licensed staff on following treatment orders/physicians orders upon admission, and readmission orders. 5. DON/designee to audit physician's orders including readmission orders 5x/week for 2 weeks, then 3x/week for 2 weeks, and then monthly. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.20(g)(h)(i)(j) REQUIREMENT Accuracy of Assessments:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.20(g) Accuracy of Assessments.
The assessment must accurately reflect the resident's status.

§483.20(h) Coordination. A registered nurse must conduct or coordinate each assessment with the appropriate participation of health professionals.

§483.20(i) Certification.
§483.20(i)(1) A registered nurse must sign and certify that the assessment is completed.
§483.20(i)(2) Each individual who completes a portion of the assessment must sign and certify the accuracy of that portion of the assessment.

§483.20(j) Penalty for Falsification.
§483.20(j)(1) Under Medicare and Medicaid, an individual who willfully and knowingly-
(i) Certifies a material and false statement in a resident assessment is subject to a civil money penalty of not more than $1,000 for each assessment; or
(ii) Causes another individual to certify a material and false statement in a resident assessment is subject to a civil money penalty or not more than $5,000 for each assessment.
§483.20(j)(2) Clinical disagreement does not constitute a material and false statement.
Observations: Based on review of the Resident Assessment Instrument User's Manual and clinical records, and staff interview, it was determined that the facility failed to make certain that comprehensive Minimum Data Set assessments were accurate and fully completed for six of nine residents (Resident R7, R8, R16, R17, R41 and R8). Findings include: The Long-Term Care Facility Resident Assessment Instrument (RAI) User's Manual, which gives instructions for completing Minimum Data Set Assessments (MDS - periodic assessment of care needs) dated October 2025, indicated that Section C: Cognitive Patterns, Question C0100 "Should Brief Interview for Mental Status Be Conducted?" (BIMS) should be coded as "0" if the resident is rarely/never understood, or it should be coded "1", and the BIMS assessment should be completed if the resident is at least sometimes understood. Section D: Mood, Question D0100 "Should Resident Mood Interview Be Conducted?" should be coded as "0" if the resident is rarely/never understood, and or it should be coded "1", and the assessment should be completed if the resident is at least sometimes understood. Section GG Mobility, indicated for how much assistance a resident requires for all mobility, eating and transfers. -Resident R7 had an MDS completed on 12/16/25. Review of Section B: Hearing, Speech, and Vision, Question B0700 indicated that Resident R8 is "understood." Review of Section C: Cognitive Patterns, Question C0100 indicated that Resident R7 is rarely understood, and the BIMS assessment was not completed. Review of Section D: Mood, Question D0100 indicated that Resident R7 is rarely understood, and the Resident Mood Interview assessment was not completed. -Resident R8 had an MDS completed on 2/14/26. Review of Section B: Hearing, Speech, and Vision, Question B0700 indicated that Resident R8 is "sometimes understood." Review of Section C: Cognitive Patterns, Question C0100 indicated that Resident R8 is rarely understood, and the BIMS assessment was not completed. Review of Section D: Mood, Question D0100 indicated that Resident R8 is rarely understood, and the Resident Mood Interview assessment was not completed. -Resident R16 had an MDS completed on 1/29/26. Review of Section B: Hearing, Speech, and Vision, Question B0700 indicated that Resident R13 is "sometimes understood." Review of Section C: Cognitive Patterns, Question C0100 indicated that Resident R16 is rarely understood, and the BIMS assessment was not completed. Review of Section D: Mood, Question D0100 indicated that Resident R16 is rarely understood, and the Resident Mood Interview assessment was not completed. -Resident R17 had an MDS completed on 2/11/26. Review of Section B: Hearing, Speech, and Vision, Question B0700 indicated that Resident R29 is "sometimes understood." Review of Section C: Cognitive Patterns, Question C0100 indicated that Resident R29 is rarely understood, and the BIMS assessment was not completed. Review of Section D: Mood, Question D0100 indicated that Resident R29 is rarely understood, and the Resident Mood Interview assessment was not completed. -Resident R41 had an MDS completed on 2/13/26. Review of Section B: Hearing, Speech, and Vision, Question B0700 indicated that Resident R40 is "understood." Review of Section C: Cognitive Patterns, Question C0100 indicated that Resident R41 is rarely understood, and the BIMS assessment was not completed. Review of Section D: Mood, Question D0100 indicated that Resident R41 is rarely understood, and the Resident Mood Interview assessment was not completed. - Resident R8 had an MDS completed on 12/21/25. Review of Section GG Functional Abilities Section 0130 Question Self Care indicated that Resident R8 is "05" set up or clean up assistance. Section 0170 question Mobility rolling left to right indicated that Resident R8 is "02" substantial/maximal assistance for rolling left to right in bed for care. - Review of Resident R8's Documentation Survey Report V2(report that is produced from the Nurse Aide documented actual care provided and used when completing Section GG on the MDS) identified Resident R8 as "01" Dependent (the helper does all the effort). -Review of Resident R8's Documentation Survey Report VS identified Resident R8 as "01" Dependent for bed mobility rolling left to right for care. During an interview on 3/6/26, at approximately 11:30 a.m. the Resident Nurse Assessment Coordinator confirmed that the above Minimum Data Set assessments were inaccurate. During an interview on 3/6/26, at approximately 1:00 p.m. the Nursing Home Administrator confirmed that the facility failed to make certain that comprehensive Minimum Data Set assessments were accurate and fully completed for five of nine residents. 28 Pa. Code: 211.5(f) Clinical records.
 Plan of Correction - To be completed: 04/14/2026

The resident R 7, 8, 16,17, and 41 had no negative outcome for not meeting the requirements for accurate coding on the MDS.2. The RNAC has been provided education by the Regional VP of Case Management/ designee.3. A lookback audit of current residents MDS of mood and cognition were reviewed for accuracy. 4. Registered Nurse Assessment Coordinator or designee will audit coding of cognition of three resident's weekly times two weeks and monthly times two months. 5. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met
483.12(c)(2)-(4) REQUIREMENT Investigate/Prevent/Correct Alleged Violation:This is a less serious (but not lowest level) deficiency and affects more than a limited number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status. This deficiency was not found to be throughout this facility.
§483.12(c) In response to allegations of abuse, neglect, exploitation, or mistreatment, the facility must:

§483.12(c)(2) Have evidence that all alleged violations are thoroughly investigated.

§483.12(c)(3) Prevent further potential abuse, neglect, exploitation, or mistreatment while the investigation is in progress.

§483.12(c)(4) Report the results of all investigations to the administrator or his or her designated representative and to other officials in accordance with State law, including to the State Survey Agency, within 5 working days of the incident, and if the alleged violation is verified appropriate corrective action must be taken.
Observations: Based on review of facility policy, clinical records, and staff interview, it was determined that the facility failed to conduct a thorough investigation of an injury obtained during care to eliminate possible neglect for one of two residents (Resident R8). Findings include: Review of facility policy "Identifying Types of Abuse" reviewed 1/8/26 with a previous review date of 14/25, Abuse is defined as the willful infliction of injury, unreasonable confinement, intimidation, or punishment with resulting physical harm, pain or mental anguish. Abuse also includes the deprivation by an individual, including a caretaker of goods or services that are necessary to attain or maintain physical, mental, and psychosocial well-being. Instances of abuse of all residents, irrespective of any mental or physical condition, cause physical harm, pain or mental anguish. It includes verbal abuse, sexual abuse, physical abuse, and mental abuse including abuse facilitated or enabled through the use of technology. Neglect as defined as, means the failure of the facility, its employees or service providers to provide goods and services to a resident that are necessary to avoid physical harm, pain, mental anguish or emotional distress. Review of the facility policy "Accidents and Incidents- Investigating and Reporting" dared 1/8/26, with a previous review date of 1/14/25, indicated that all accidents and incidents involving residents, employees, etc., occurring on the premises shall be investigated and reported to the Administrator. The Nurse Supervisor shall promptly initiate and document the investigation of the accident or incident. Review of the clinical record indicated Resident R8 was admitted to the facility on 1/25/24. Review Resident R8's Minimum Data Set (MDS - periodic assessment of resident care needs) dated 2/14/26, indicated diagnoses of dementia, psychotic and mood disturbances, anxiety, obesity and dysphagia. Review of Resident R8's MDS dated 12/21/25, indicated substantial/maximal assistance for bed mobility. During a clinical record review, a progress note dated 1/7/26, indicated Resident R8 had a fall out of bed when being provided care which resulted in a laceration above her eyebrow which required treatment. Review of Resident R8's plan of care for "Falls" indicated resident is at risk for falls and to provide assistance as required. Bilateral fall mats to be in place. During an observation on 3/4/26, at 3:00 p.m., fall mat on right side of bed close to wall and leaning onto wall, no mat on left side of bed and Resident R8 had legs bent leaning towards left side of bed. During an observation on 3/5/26, at 9:00 a.m., fall mat on right side of bed unmoved from previous day and no mat on left side of bed. During an interview on 3/4/25, at 3:00 p.m., Registered Nurse Employee E6 and Nurse Aide (NA) Employee E7 stated that substantial/ maximal assistance requires two staff. During an interview on 3/5/26, at 9:00 a.m., NA Employee E8 stated that substantial/maximal assistance requires two staff. During an interview on 3/5/26, at 10:58 a.m., Therapy Manager Employee E9 stated that Resident R8 was not on caseload since 10/9/25, due to her inability to understand and follow commands and that care was identified to require two staff at all times due to her dementia progression. During an interview on 3/5/26, at 10:28 a.m., the Nursing Home Administrator confirmed that the facility failed to identify andconduct a thorough investigation of an injury obtained during care to eliminate possible neglect for one of five residents (Resident R8). 28 Pa Code: 201.18 (e)(1)(2) Management. 28 Pa Code: 201.29 (a)(c) Resident Rights. 28 Pa Code: 211.12 (a)(c)(d)(1)(3)(5) Nursing services.
 Plan of Correction - To be completed: 04/14/2026

During annual survey the Resident R8 had bilateral fall mats placed. Review of the residents care plan and Kardex showed that the resident was listed as an assist of 1 for bed mobility and the CNA followed the documented care plan. Therapy evaluated residents assistance need for bed mobility and deemed her to be an assist of 2 for bed mobility. CNO educated the NHA, DON and HR on identifying and reporting abuse and neglect and proper steps for investigating allegations. DON or designee will educate facility staff on "identifying abuse and neglect" to ensure all staff are aware of the policy and procedure and follow them accurately. Audits: DON or designee will audit the risk events 5 times weekly times 2 weeks, weekly times 2 weeks and monthly times 1 month to ensure any events that could be abuse or neglect are investigated and reported properly. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.10(a)(1)(2)(b)(1)(2) REQUIREMENT Resident Rights/Exercise of Rights:This is a less serious (but not lowest level) deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.10(a) Resident Rights.
The resident has a right to a dignified existence, self-determination, and communication with and access to persons and services inside and outside the facility, including those specified in this section.

§483.10(a)(1) A facility must treat each resident with respect and dignity and care for each resident in a manner and in an environment that promotes maintenance or enhancement of his or her quality of life, recognizing each resident's individuality. The facility must protect and promote the rights of the resident.

§483.10(a)(2) The facility must provide equal access to quality care regardless of diagnosis, severity of condition, or payment source. A facility must establish and maintain identical policies and practices regarding transfer, discharge, and the provision of services under the State plan for all residents regardless of payment source.

§483.10(b) Exercise of Rights.
The resident has the right to exercise his or her rights as a resident of the facility and as a citizen or resident of the United States.

§483.10(b)(1) The facility must ensure that the resident can exercise his or her rights without interference, coercion, discrimination, or reprisal from the facility.

§483.10(b)(2) The resident has the right to be free of interference, coercion, discrimination, and reprisal from the facility in exercising his or her rights and to be supported by the facility in the exercise of his or her rights as required under this subpart.
Observations: Based on review of facility policy, resident records, and resident and staff interview it was determined that the facility failed to maintain the privacy and dignity of one of six residents (Residents R3). Findings include: The facility policy "Resident Rights" dated 1/8/26, previously dated 1/14/25, indicated that facility residents have the right to a dignified existence. Review of the clinical record indicated Resident R3 was admitted to the facility on 4/10/21. Review of the Minimum Data Set (MDS - periodic assessment of resident care needs) dated 1/25/26, included Crohn's disease (chronic inflammatory bowel disease (IBD) causing severe, long-term inflammation) and history of a stroke. Review of Section C: Cognitive Patterns indicated Resident R3 was cognitively intact. During an interview completed on 3/5/26, at 9:08 a.m. Resident R3 stated that she was uncomfortable using the shower room on her nursing unit because a male resident's room opens directly into the shower room through an unlocked door. Observation of the Garden unit shower room revealed that it was directly accessed from Resident R20 through an internal door in the shower room. Review of Resident R20's clinical record revealed that he was mobile in his wheelchair. During an interview on 3/5/26, at approximately 10:30 a.m. the Nursing Home Administrator confirmed that the facility failed to uphold the privacy and dignity of one of six residents. 28 Pa Code: 201.29 (i) Resident rights.
 Plan of Correction - To be completed: 04/14/2026

The Facility immediately changed the door handle on the shower room door to have a lock that will be locked during all shower times. DON will educate Direct care staff will be educated on resident rights and utilizing new lock. Audits will be conducted by the Administrator or designee weekly for four weeks to ensure lock is being utilized appropriately. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.45(g)(h)(1)(2) REQUIREMENT Label/Store Drugs and Biologicals:This is a less serious (but not lowest level) deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.45(g) Labeling of Drugs and Biologicals
Drugs and biologicals used in the facility must be labeled in accordance with currently accepted professional principles, and include the appropriate accessory and cautionary instructions, and the expiration date when applicable.

§483.45(h) Storage of Drugs and Biologicals

§483.45(h)(1) In accordance with State and Federal laws, the facility must store all drugs and biologicals in locked compartments under proper temperature controls, and permit only authorized personnel to have access to the keys.

§483.45(h)(2) The facility must provide separately locked, permanently affixed compartments for storage of controlled drugs listed in Schedule II of the Comprehensive Drug Abuse Prevention and Control Act of 1976 and other drugs subject to abuse, except when the facility uses single unit package drug distribution systems in which the quantity stored is minimal and a missing dose can be readily detected.
Observations: Based on observation, facility policy review, and staff interviews, it was determined that the facility failed to ensure opened vials were labeled in accordance with currently accepted professional principles for one of one medication rooms(Fawn Medication Room) and medications obtained from the emergency machine for a resident were labeled in accordance with currently accepted professional standards for one of two medication carts ( Fawn Medication Cart). Findings include: Review of facility policy "Medication Labeling and Storage," dated 1/8/26, with a previous review date of 1/14/25, indicated multi-dose vials that have been opened or accessed (e.g., needle punctured) are dated and discarded within 28 days unless the manufacturer specifies a shorter or longer date for the open vial. Labeling of medications dispensed by the pharmacy is consistent with applicable federal and state requirements. During observation of the Fawn medication storage room on 3/4/26, at 11:08 a.m., revealed one vial of tuberculosis purified protein derivative solution (PPD - used to determine resident or staff exposure or infection with tuberculosis) opened with no opened date written on the vial or the box that contained the vial. During an interview on 3/4/26, at 11:08 a.m., Registered Nurse Employee E5 confirmed that the one vial appeared accessed and that there was not an open date on the vial or box of the PPD solution. During an observation on 3/5/26, at 7:40 a.m., Registered Nurse Employee E4 removed a Nicotine Patch box containing an opened undated patch and stated that was the patch used for Resident R49. RN Employee E4 confirmed the box and parch were unlabeled and undated. 29 Pa code 211.12(d)(1)(5) Nursing services
 Plan of Correction - To be completed: 04/14/2026

The residents had no negative outcome from the PPD vial that didn't have an open date or the unused open Nicotine Patch box; both were immediately removed. All nursing staff will be educated on dating medications and labels by DON. Audits will be conducted by the DON or designee weekly for four weeks and monthly by 2 months to ensure medications are properly dated and labeled. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.21(b)(1)(3) REQUIREMENT Develop/Implement Comprehensive Care Plan:This is a less serious (but not lowest level) deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.21(b) Comprehensive Care Plans
§483.21(b)(1) The facility must develop and implement a comprehensive person-centered care plan for each resident, consistent with the resident rights set forth at §483.10(c)(2) and §483.10(c)(3), that includes measurable objectives and timeframes to meet a resident's medical, nursing, and mental and psychosocial needs that are identified in the comprehensive assessment. The comprehensive care plan must describe the following -
(i) The services that are to be furnished to attain or maintain the resident's highest practicable physical, mental, and psychosocial well-being as required under §483.24, §483.25 or §483.40; and
(ii) Any services that would otherwise be required under §483.24, §483.25 or §483.40 but are not provided due to the resident's exercise of rights under §483.10, including the right to refuse treatment under §483.10(c)(6).
(iii) Any specialized services or specialized rehabilitative services the nursing facility will provide as a result of PASARR recommendations. If a facility disagrees with the findings of the PASARR, it must indicate its rationale in the resident's medical record.
(iv)In consultation with the resident and the resident's representative(s)-
(A) The resident's goals for admission and desired outcomes.
(B) The resident's preference and potential for future discharge. Facilities must document whether the resident's desire to return to the community was assessed and any referrals to local contact agencies and/or other appropriate entities, for this purpose.
(C) Discharge plans in the comprehensive care plan, as appropriate, in accordance with the requirements set forth in paragraph (c) of this section.
§483.21(b)(3) The services provided or arranged by the facility, as outlined by the comprehensive care plan, must-
(iii) Be culturally-competent and trauma-informed.
Observations: Based on a review facility policy, clinical records, and staff interviews, it was determined that the facility failed to develop person-centered care plans for one of six residents (Resident R41). Findings include: The Long-Term Care Facility Resident Assessment Instrument (RAI) User's Manual, which gives instructions for completing Minimum Data Set Assessments (MDS - periodic assessment of care needs) dated October 2025, indicated that Section V: Care Area Assessment (CAA) Summary instructions stated, "For each triggered care area, Column B "Care Planning Decision" is checked to indicate that a new care plan, care plan revision, or continuation of the current care plan is necessary to address the issue(s) identified in the assessment of that care area." Review of the facility policy "Care Plans, Comprehensive Person-Centered" dated 1/8/26, previously dated 1/14/25, indicated, "A comprehensive, person-centered care plan that includes measurable objectives and timetables to meet the resident's physical, psychosocial, and functional needs is developed and implemented for each resident." Review of the clinical record indicated Resident R41 was admitted on 11/11/22. Review of Resident R41's MDS dated 2/13/26, indicated diagnoses of dementia, depression, and chronic pain. Review of Resident R41's comprehensive MDS dated 11/13/25, indicated psychotropic drug use was triggered in Section V: Care Area Assessment Summary. Review of the CAA Worksheet included the question, "Will Psychotropic Drug Use be addressed in the care plan?" This question was documented as "Yes." Review of Resident R41's physician order dated 5/16/24, indicated to administer venlafaxine (an anti-depressant medication) 37.5 mg and 75 mg daily for depression. Review of Resident R41's physician order dated 11/25/25, indicated to administer haloperidol 0.5mg every twelve hours PRN for agitation. Review of Residents R41 care plan initiated 11/11/22, most recently revised 2/23/26, failed to include a plan of care developed for psychotropic drug use. During an interview on 3/6/26, at approximately 12:00 p.m. the Nursing Home Administrator confirmed the facility failed to develop person-centered care plans for one of six residents. 28 Pa. Code: 211.12 (d) (1) (2) (5) Nursing services.
 Plan of Correction - To be completed: 04/14/2026

The resident R 41comprehensive care plans were updated to reflect current use of psychoactive medications. Review of current residents with psychoactive medications care plans were reviewed for accuracy. DON to educate Licensed staff on facility comprehensive care plan policy. DON or designee will audit five residents weekly times two weeks and monthly times two months residents careplans for accuracy. The results of these audits will be reported to the Facility's Monthly QAPI meeting until substantial compliance is met
483.10(g)(5)(i)(ii) REQUIREMENT Required Postings:Least serious deficiency but was found to be widespread throughout the facility and/or has the potential to affect a large portion or all the residents. This deficiency has the potential for causing no more than a minor negative impact on the resident.
§483.10(g)(5) The facility must post, in a form and manner accessible and understandable to residents, resident representatives:
(i) A list of names, addresses (mailing and email), and telephone numbers of all pertinent State agencies and advocacy groups, such as the State Survey Agency, the State licensure office, adult protective services where state law provides for jurisdiction in long-term care facilities, the Office of the State Long-Term Care Ombudsman program, the protection and advocacy network, home and community based service programs, and the Medicaid Fraud Control Unit; and
(ii) A statement that the resident may file a complaint with the State Survey Agency concerning any suspected violation of state or federal nursing facility regulation, including but not limited to resident abuse, neglect, exploitation, misappropriation of resident property in the facility, and non-compliance with the advanced directives requirements (42 CFR part 489 subpart I) and requests for information regarding returning to the community.
Observations: Based on observations and staff interview, it was determined the facility failed to post contact information for the Medicaid Fraud Unit on two of two nursing units (Fawn and Garden nursing units). Findings include: During observations conducted on 3/4/25, at approximately 1:30 p.m. of the Fawn and Garden nursing units revealed the facility revealed the facility did not have the Medicaid Fraud Unit contact information posted or accessible to residents. During an interview on 3/6/26, at approximately 12:00 p.m., the Nursing Home Administrator confirmed the facility failed to post contact information for the Medicaid Fraud on two of two nursing units. 28 Pa. Code: Resident rights.
 Plan of Correction - To be completed: 04/14/2026

Postings for Medicaid Fraud Unit contact information were posted and accessible to residents. The Administrator will be educated on Medicaid Fraud Unit to be posted in facility by clinical nursing officer. Audits will be conducted by the Administrator or designee weekly for four weeks to ensure Medicaid Fraud Unit postings are accessible by residents. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.10(g)(13) REQUIREMENT Posting/Notice of Medicare/Medicaid on Admit:Least serious deficiency but was found to be widespread throughout the facility and/or has the potential to affect a large portion or all the residents. This deficiency has the potential for causing no more than a minor negative impact on the resident.
§483.10(g)(13) The facility must display in the facility written information, and provide to residents and applicants for admission, oral and written information about how to apply for and use Medicare and Medicaid benefits, and how to receive refunds for previous payments covered by such benefits.
Observations: Based on observations and staff interview, it was determined the facility failed to display written information on applying for Medicare and Medicaid benefits and receiving refunds for previous payments covered by Medicare and Medicaid on two of two nursing units (Fawn and Garden nursing units). Findings include: Observations conducted on 3/4/25, at approximately 1:30 p.m. of the Fawn and Garden nursing units, revealed the facility failed to include information on how to apply for Medicare and Medicaid benefits and receiving refunds for previous payments covered by Medicare and Medicaid . During an interview on 3/6/26, at approximately 12:00 p.m., the Nursing Home Administrator confirmed the facility failed to display written information on applying for Medicare and Medicaid benefits and receiving refunds for previous payments covered by Medicare and Medicaid on two of two nursing units. 28 Pa. Code: Resident rights.
 Plan of Correction - To be completed: 04/14/2026

Posting for how to apply for Medicare and Medicaid benefits and receiving refunds for previous payments covered by Medicare and Medicaid were posted accessible to residents. The Administrator will be educated on required postings for how to apply for Medicare and Medicaid benefits and receiving refunds for previous payments covered by Medicare and Medicaid to be posted in facility by the clinical nursing officer. Audits will be conducted by the Administrator or designee weekly for four weeks to ensure required postings are accessible by residents. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.10(g)(10)(11) REQUIREMENT Right to Survey Results/Advocate Agency Info:Least serious deficiency but affects more than a limited number of residents, staff, or occurrences. This deficiency has the potential for causing no more than a minor negative impact on the resident but is not found to be throughout this facility.
§483.10(g)(10) The resident has the right to-
(i) Examine the results of the most recent survey of the facility conducted by Federal or State surveyors and any plan of correction in effect with respect to the facility; and
(ii) Receive information from agencies acting as client advocates, and be afforded the opportunity to contact these agencies.

§483.10(g)(11) The facility must--
(i) Post in a place readily accessible to residents, and family members and legal representatives of residents, the results of the most recent survey of the facility.
(ii) Have reports with respect to any surveys, certifications, and complaint investigations made respecting the facility during the 3 preceding years, and any plan of correction in effect with respect to the facility, available for any individual to review upon request; and
(iii) Post notice of the availability of such reports in areas of the facility that are prominent and accessible to the public.
(iv) The facility shall not make available identifying information about complainants or residents.
Observations: Based on observation and staff interview, it was determined that the facility failed to post the most recent Federal or State survey results for one of one survey books observed (located in main entrance lobby). Findings Include: Observation of the survey binder located in the main entrance lobby on 3/4/26, at 1:30 p.m, revealed the most recent survey results present were dated 9/11/24. Review of the facility's survey history revealed surveys dated: 1/8/25, 4/30/25, 6/11/25, 7/28/25, 9/3/25, 11/4/25, 12/2/25, 1/14/26, and 2/12/26. During an interview on 3/6/26, at approximately 12:00 p.m. the Nursing Home Administrator confirmed the facility failed to post the most recent Federal or State survey results for one of one survey books. 28 Pa. Code 201.14 Responsibility of licensee
 Plan of Correction - To be completed: 04/14/2026

Current survey results were added to the survey binder. Administrator will be educated on right to view survey results by clinical nursing officer. Audits will be conducted by the Administrator or designee weekly for four weeks to ensure survey postings are available for review. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.
483.20(f)(1)-(4) REQUIREMENT Encoding/Transmitting Resident Assessments:Least serious deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency has the potential for causing no more than a minor negative impact on the resident.
§483.20(f) Automated data processing requirement-
§483.20(f)(1) Encoding data. Within 7 days after a facility completes a resident's assessment, a facility must encode the following information for each resident in the facility:
(i) Admission assessment.
(ii) Annual assessment updates.
(iii) Significant change in status assessments.
(iv) Quarterly review assessments.
(v) A subset of items upon a resident's transfer, reentry, discharge, and death.
(vi) Background (face-sheet) information, if there is no admission assessment.

§483.20(f)(2) Transmitting data. Within 7 days after a facility completes a resident's assessment, a facility must be capable of transmitting to the CMS System information for each resident contained in the MDS in a format that conforms to standard record layouts and data dictionaries, and that passes standardized edits defined by CMS and the State.

§483.20(f)(3) Transmittal requirements. Within 14 days after a facility completes a resident's assessment, a facility must electronically transmit encoded, accurate, and complete MDS data to the CMS System, including the following:
(i)Admission assessment.
(ii) Annual assessment.
(iii) Significant change in status assessment.
(iv) Significant correction of prior full assessment.
(v) Significant correction of prior quarterly assessment.
(vi) Quarterly review.
(vii) A subset of items upon a resident's transfer, reentry, discharge, and death.
(viii) Background (face-sheet) information, for an initial transmission of MDS data on resident that does not have an admission assessment.

§483.20(f)(4) Data format. The facility must transmit data in the format specified by CMS or, for a State which has an alternate RAI approved by CMS, in the format specified by the State and approved by CMS.
Observations: Based on review of the Long-Term Care Resident Assessment Instrument User's Manual, clinical records, and staff interview, it was determined that the facility failed to transmit Minimum Data Set's (MDS -periodic assessment of care needs) to the required electronic system within the mandated time frame for one of five residents reviewed (Resident R18). Findings include: The Long-Term Care Facility Resident Assessment Instrument (RAI) User's Manual, which provides instructions and guidelines for completing required MDS assessments, dated October 2025, indicated that Entry, Death and Facility and Discharge tracking MDS assessments must be completed and transmitted within 14 days of the event date. Resident R18 had a discharge date of 9/6/25. Further review of the clinical record failed to reveal a discharge MDS completed for Resident R18. During an interview on 3/6/26, at approximately 11:30 a.m. the Resident Nurse Assessment Coordinator Employee E1 confirmed the above assessment was not completed, due to a lack of sufficient staff. During an interview on 3/6/26, at approximately 12:00 p.m. the Nursing Home Administrator confirmed that the facility failed to transmit MDS assessments to the required electronic system within the mandated time frame for one of 16 residents reviewed. 28 Pa. Code 211.5(d) Medical records.
 Plan of Correction - To be completed: 04/14/2026

The resident R18 ceased to breath in September 2025, and a late assessment was completed in October outside of the 14 day requirement. No other residents were affected by this deficient practice. The Registered nurse assessment coordinator will be educated on (RAI) User's Manual, which provides instructions and guidelines for completing required MDS assessments that need to be completed and submitted within 14 days by Regional RNAC. The NHA/designee will audit weekly MDS to ensure that they were completed and submitted within 14 days weekly x 2 weeks then biweekly x 2 weeks then monthly x 1 month. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met
§ 211.12(f.1)(4) LICENSURE Nursing services. :State only Deficiency.
(4) Effective July 1, 2023, a minimum of 1 LPN per 25 residents during the day, 1 LPN per 30 residents during the evening, and 1 LPN per 40 residents overnight.
Observations: Based on review of nursing time schedules and staff interviews it was determined that the facility administrative staff failed to provide a minimum of one licensed practical nurse (LPN) per 25 residents during the day shift, per 30 residents during the evening shift, and per 40 residents during the night shift on 16 of 21 days (2/13/26, 2/14/26, 2/15/26, 2/16/26. 2/17/26, 2/18/26, 2/20/26, 2/21/26, 2/22/26, 2/23/26, 2/24/26, 2/25/26, 2/26/26, 2/27/26, 2/28/26, and 3/1/26). Findings include: Review of facility census data, nursing time schedules, and deployment sheets from 2/13/26, through 3/5/25, revealed the following LPN staffing shortages. -2/13/26, Census 38, day shift short 3.66 hours and evening shift short 1.63 hours for LPNs. -2/14/26, Census 38, evening shift short 1.63 hours for LPNs. -2/15/26, Census 38, day shift short 4.16 hours for LPNs. -2/16/26, Census 38, evening shift short 1.88 hours for LPNs. -2/17/26, Census 37, evening shift short 1.37 hours for LPNs. -2/18/26, Census 36, evening shift short 1.1 hours for LPNs. -2/20/26, Census 38, day shift short 2.08 hours and evening shift short 0.48 hours for LPNs. -2/21/26, Census 38, day shift short 4.16 and evening shift short 1.63 hours for LPNs. -2/22/26, Census 38, day shift short 3.91 hours for LPNs. -2/23/26, Census 38, day shift short 3.96 hours for LPNs. -2/24/26, Census 39, day shift short 0.93 and evening shift short 1.65 hours for LPNs. -2/25/26, Census 40, day shift short 3.05 and evening shift short 2.17 hours for LPNs. -2/26/26, Census 40, day shift short 5.3 hours and evening shift short 2.17 hours for LPNs. -2/27/26, Census 40, day shift short 5.55 hours for LPNs. -2/28/26, Census 40, day shift short 4.8 hours for LPNs. -3/1/26, Census 36, day shift short 3.02 hours for LPNs. During an interview on 3/5/26, at 1:18 p.m., the Nursing Home Administrator confirmed the facility failed to provide a minimum of one licensed practical nurse per 25 residents during the day shift, per 30 residents during the evening shift, and per 40 residents during the night shift on 16 of 21 days.
 Plan of Correction - To be completed: 04/14/2026

The residents had no negative outcome for not meeting a minimum of 1 LPN per 25 residents during the day, 1 LPN per 30 residents during the evening, and 1 LPN per 40 residents overnight. The facility is attempting to hire additional staff as well as holding daily staffing meetings to track staffing 5x a week. DON/designee will provide the Staffing Coordinator/HR with re-education on the Pennsylvania staffing requirements for ratios. Staffing coordinator/designee will audit the ratios five times weekly for 2 weeks and monthly times two month. The results will be reviewed at the Quality Assurance and Process Improvement meetings until substantial compliance has been met.

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