Above average — CMS composite of the measures below.
The next survey window likely opens around December 2026
Estimate from public CMS data, current as of July 2026. Survey timing is at the state agency's discretion.
Citation history
Health deficiencies cited at Cherry Hill Manor during CMS and state inspections, most recent first.
A hospice resident with severe cognitive impairment, COPD, CHF, and a documented comfort‑focused care goal experienced unmanaged pain and terminal agitation when PRN morphine and lorazepam ordered for pain, SOB, and anxiety were not administered in a timely manner. A provider ordered sublingual morphine and lorazepam intensol early in the afternoon, and a hospice RN later documented that the resident was actively dying with severe pain, moaning, labored breathing, and terminal agitation, noting that pain management was ineffective and that the unit LPN was seeking an override for needed medications. MAR review showed morphine was not given until several hours after the order and after the hospice assessment, and lorazepam was delayed even longer, despite both drugs being available in the Omnicell and E‑Kit. In interviews, the LPN stated she did not feel the resident needed morphine and waited for a pharmacy code, and she did not consider the E‑Kit lorazepam, while the DON acknowledged the facility nurse was responsible for assessing and administering PRN medications and could not show that care met professional standards; a family member reported the resident appeared to be in agonizing pain and anxiety during this period.
A facility failed to notify three residents in writing when their personal needs fund balances reached the Medicaid resource threshold. Record review showed all three accounts exceeded the $4,000 limit, and the ABOM could not provide evidence that written notice had been given when the balances reached $200 below the SSI resource guideline.
A survey results binder stored in the lobby was accessible to the public and contained a resident roster attached to the statement of deficiencies. The roster identified four residents by number and included information such as physician orders and medical diagnoses. The Administrator acknowledged that the residents' names and corresponding identifiers were included in the binder and should not have been.
A resident with intact cognition and significant ADL dependence developed a skin tear to the elbow that was dressed without a documented order. Surveyors observed the dressing with drainage over multiple days, but the record lacked wound documentation and evidence that the provider was notified when the impairment was first identified. Staff later stated they had only just become aware of the wound, and the wound was then measured as three skin tear areas totaling 3 cm by 3 cm.
Failure to document and off-load a resident’s left heel skin impairment. A resident with dementia, muscle weakness, and hospice services had orders for heel skin prep, dressing care for a left heel blister, and heel boots for boggy heels. Surveyors observed the resident multiple times without the ordered heel boots, and the record lacked measurements and descriptions of the left heel impairment. Staff interviews showed the NA was unaware of the heel boot order, the LPN did not replace the boots after treatment, and the DON and wound nurse could not provide evidence that the impairment was documented or that the boots were applied as ordered.
A resident with hypotension and ESRD received Midodrine outside the ordered BP hold parameters. The MAR showed the medication was administered when systolic BP was above 130, and the LPN stated that if it was documented as completed, it was given. The DON could not provide evidence that the medication had been held as ordered.
Incomplete MAR and skin documentation were identified for two residents. One resident with hypotension had Midodrine documented as given despite BP readings above the hold parameter, and the MAR was later altered after staff said the doses were not actually administered. Another resident with a left heel blister/callous had treatment orders in place, but weekly skin checks did not consistently document the heel impairment, even though surveyors observed a hardened non-blanchable area and the ADNS acknowledged the omission.
A resident admitted after spinal surgery with a Hemovac drain and surgical wound did not have a baseline care plan developed within 48 hours that addressed care instructions for the wound or drain. Nursing leadership confirmed the omission when interviewed, and the resident was later hospitalized after presenting with signs of infection.
A resident with a Hemovac drain following spinal surgery did not have their drain output monitored or documented as required by facility policy. There were no physician orders for drain management, and staff could not provide evidence of required monitoring or documentation. This failure was confirmed by interviews with nursing staff, the DON, and the facility physician, as well as by the lack of documentation provided to the surgeon's office.
Two LPNs provided care to a resident with a Hemovac drain following spinal surgery without having received training or competency assessment specific to Hemovac drain care, as confirmed by staff interviews and facility records. The facility did not provide required education or competencies for this procedure, despite policy and resident needs.
A facility failed to implement Enhanced Barrier Precautions (EBP) for a resident with a wound requiring dressing. Despite signage indicating the need for gown and glove use during high-contact care activities, staff were observed not adhering to these precautions. Interviews revealed a lack of understanding and adherence to the EBP policy, and the facility was unable to provide evidence of consistent EBP implementation.
Failure to Provide Timely End‑of‑Life Pain and Anxiety Management for a Hospice Resident
Penalty
Summary
The deficiency involves the facility’s failure to provide timely and appropriate end‑of‑life pain and symptom management for a hospice resident in accordance with physician orders and professional standards of practice. The resident was admitted with multiple chronic conditions, including COPD and CHF, and had severe cognitive impairment, requiring moderate to maximum assistance with ADLs. A provider note documented that the resident had recently presented with fever, shortness of breath, hypoxia, lethargy, and crackles throughout the lungs, and that the family’s and resident’s primary goal of care was comfort. The provider discussed hospice with the family, obtained consent for PRN morphine, lorazepam, and atropine drops for comfort, and sent a hospice referral, with the expectation that hospice would assess the resident that evening. Physician orders were entered for lorazepam intensol 0.25 mL every 4 hours PRN for anxiety/agitation and morphine 0.25 mL every 4 hours PRN for pain/shortness of breath early in the afternoon. A hospice RN assessed the resident later that day and documented that the resident was actively dying, with abnormal vital signs, severe pain (pain score 7/10), moaning, labored breathing, hyperventilation episodes, loud moaning or groaning, crying, and inability to be consoled, as well as agitation, disorientation, lethargy, and restlessness attributed to terminal agitation. The hospice RN noted that an order for sublingual morphine had been written earlier in the day but that the medication had not yet arrived from the pharmacy, and that the unit LPN was calling to obtain an override for needed medications. The hospice RN documented that current pain management was not effective and that they were awaiting morphine from the pharmacy. Medication administration records showed that morphine was not administered until 6:39 PM, approximately four and a half hours after it was ordered and about two hours after the hospice nurse’s assessment documenting severe pain. Lorazepam intensol was not administered until 10:40 PM, approximately nine hours after it was ordered and about six and a half hours after the hospice nurse’s assessment documenting anxiety and terminal agitation. Review of the Omnicell and the emergency E‑Kit showed that morphine and lorazepam intensol were available in the facility and could have been administered earlier. In interviews, the hospice nurse reported that the resident had periods of extreme anxiety and agitation and that the LPN stated she was waiting for a code from the pharmacy before administering morphine. The LPN who cared for the resident during the 3 PM–11 PM shift stated that the resident was sweaty, warm, reaching out for people’s hands, and had arthritis pain, and that she did not feel the resident needed morphine, so she waited to get a code from the pharmacy and administered it later in the evening; she also stated she did not think about the availability of lorazepam intensol in the E‑Kit. The DON acknowledged that the hospice nurse is not employed by the facility and that the facility nurse is responsible for assessing the resident and administering PRN medications, and could not provide evidence that the resident received treatment and care in accordance with professional standards of practice for end‑of‑life medications. Additionally, earlier in the resident’s course, a progress note documented that hospice services had been discussed with the family and that an informational consult in Spanish was requested, with the writer indicating an intent to contact hospice agencies to advocate for that request. Record review did not show evidence that the facility contacted a hospice agency to facilitate the requested informational consultation in Spanish at that time. The hospice agency’s director later reported that the agency did not receive a referral for the resident prior to the date the resident was ultimately admitted to hospice. A family member complainant reported that on the afternoon before the resident’s death there was a delay in providing the ordered morphine and lorazepam, that the resident appeared to be in agonizing pain and anxiety, and that the resident’s feet were hanging off the bed when the family member entered the room. The facility’s failure to use available medications from the Omnicell and E‑Kit and to administer ordered morphine and lorazepam in a timely manner, despite clear signs of severe pain and terminal agitation and the established comfort‑focused goals of care, led to unmanaged pain, terminal agitation, and psychosocial distress during the resident’s final hours of life.
Failure to Notify Residents of Excess Personal Needs Fund Balances
Penalty
Summary
The facility failed to notify residents, or resident representatives, in writing when resident personal needs account balances reached $200 less than the SSI Medicaid resource eligibility limit. Based on record review, three residents with facility-handled personal needs funds had balances above the $4,000 limit: Resident ID #65 had $4,067.67, Resident ID #77 had $4,171.23, and Resident ID #159 had $7,053.36. The applicable Medicaid LTSS procedure requires written notification when the account balance reaches $200 below the resource eligibility guideline, but during interview the Assistant Business Office Manager was unable to provide evidence that these residents had been notified in writing when their balances reached that threshold.
Resident Identifiers Left in Public Survey Binder
Penalty
Summary
The facility failed to protect identifying information for four current residents when a resident-identifying document was kept in the survey results binder in the first-floor lobby, where it was accessible to the public. During surveyor observation, a black survey results binder was seen stored on a wall in the lobby. Review of the binder showed a resident roster attached to the statement of deficiencies for the survey with exit date 12/7/2023, identifying Resident ID #s 8, 46, 62, and 146. The attached rosters contained information including physician's orders and medical diagnoses. In interview, the Administrator acknowledged that the residents' names and corresponding number identifiers were included in the binder and should not have been.
Failure to Notify Provider and Document New Skin Tear
Penalty
Summary
The facility failed to ensure that treatment and care were provided in accordance with orders, resident preferences, and goals for a resident with an observed skin tear to the left elbow. The resident was admitted in February 2025 with diagnoses including hemiplegia and hemiparesis following a cerebral infarction affecting the left side, had intact cognition with a BIMS score of 15 out of 15, and required maximum assistance with activities of daily living including personal hygiene and upper body dressing. Surveyor observations found an undated white-bordered gauze dressing with visible dark drainage on the resident’s elbow on multiple occasions, and the resident stated the elbow had been hit on a wheelchair armrest and that a nurse had applied the dressing, but was unsure when it was first placed. Record review did not reveal a physician order for a dressing to the left arm, and there was no documentation describing the wound, including measurements, or showing that the provider was notified of a new skin impairment requiring a dressing. When the wound was later observed with a pink foam dressing labeled for the day shift, staff stated they had only just become aware of the skin impairment, that blood was present, and that they would notify the NP. The LPN acknowledged there was no order or prior documentation for the dressing, the unit manager stated she had just learned of the impairment, the wound nurse then measured and assessed the wound as three skin tear areas collectively measuring 3 cm by 3 cm, and the DON stated she would expect the provider to be notified when a wound is identified but could not provide evidence that notification or an order had occurred when the wound was initially identified.
Failure to Document and Off-Load a Resident’s Left Heel Skin Impairment
Penalty
Summary
The facility failed to ensure that a resident with a newly identified left heel skin impairment received necessary treatment and services consistent with professional standards of practice to promote healing, prevent infection, and prevent new ulcers from developing. The resident was admitted with diagnoses including dementia and muscle weakness, was dependent on staff for ADLs including dressing, and received hospice services. The care plan identified the resident as at risk for altered skin integrity due to impaired mobility and included interventions to assess the location and size of skin injury and report failure to heal to the provider. Physician orders dated 12/2/2025 directed staff to apply skin prep to both heels twice daily, apply skin prep to the left heel blister and cover it with a dressing every 7 days, and apply heel boots every shift for boggy heels as tolerated. Surveyor observations found the resident without heel boots on multiple occasions while in bed and while seated in the common area. Record review did not reveal evidence that the resident was unable to tolerate the heel boots, and the clinical record also lacked measurements or descriptions of the left heel skin impairment identified in the treatment order. Weekly skin checks reviewed by surveyors did not document a left heel impairment on several dates, and during observation on 1/8/2026 the resident was found to have a non-blanchable darkened skin impairment to the left heel measuring 2.4 cm x 2.3 cm. Staff interviews showed the NA was not aware the resident required bilateral heel boots and believed hospice status meant the boots were not needed, while the LPN stated she failed to put the heel boots on after completing the left heel treatment. The ADNS/wound nurse, physician, and DON all acknowledged the lack of documentation and inability to provide evidence that the heel impairment had been measured or that the heel boots were applied as ordered.
Medication Given Outside Ordered BP Parameters
Penalty
Summary
The facility failed to ensure a resident was free from significant medication errors when Midodrine HCl 2.5 mg, ordered twice daily for hypotension with instructions to hold the medication for systolic blood pressure greater than 130, was administered outside the ordered parameters. The resident was admitted with diagnoses including hypotension and end stage renal disease. Review of the December 2025 and January 2026 MAR showed the medication was given when the resident's systolic blood pressure was 133 on 12/22/2025 at 8:00 AM, 138 on 12/27/2025 at 8:00 AM, and 154 on 1/2/2026 at 6:00 PM. During interview, the Unit Manager/LPN stated that if the order was documented as completed in the MAR, then it was administered to the resident. The DON, in the presence of the Administrator, was unable to provide evidence that the medication had been held according to the ordered blood pressure parameters on those dates and times.
Incomplete Medication and Skin Integrity Documentation
Penalty
Summary
Resident ID #13, admitted with hypotension, had a physician order for Midodrine HCL 2.5 mg twice daily with instructions to hold the medication for blood pressure greater than 130. Review of the January 2026 MAR showed the medication documented as given on three occasions when the resident’s blood pressure was above the ordered parameter: 160/75, 166/73, and 144/62. During the surveyor’s interview with the DNS and Administrator, the documentation error was brought to their attention. A later review of the MAR showed the Midodrine entries had been modified, with a number 3 added to indicate the vitals were outside the administration parameters, and the DNS stated that the nurses reported they had not administered the medication and changed the documentation to reflect it was not given. Resident ID #80, admitted with adult failure to thrive and abnormalities of gait and mobility, had orders for treatment to the left heel for a blister, later changed to skin prep with a foam dressing. The resident’s weekly skin monitoring checks did not document impaired skin integrity to the left heel on multiple dates, even though a weekly skin integrity data collection form noted an alteration in skin with the description "left heel/treatment in place." On observation, surveyors noted a hardened non-blanchable area to the left heel, which the ADNS described as a callous. The ADNS acknowledged that the area was not documented on the skin checks and stated it should have been assessed and described.
Failure to Develop Baseline Care Plan for Surgical Wound and Hemovac Drain
Penalty
Summary
The facility failed to develop and implement a baseline care plan within 48 hours of admission for a resident who was admitted following spinal fusion surgery and required orthopedic aftercare. Upon admission, documentation indicated the presence of a surgical dressing on the posterior back and a Hemovac drain with serosanguineous drainage. However, review of the baseline care plan revealed no evidence of care planning related to the surgical wound or the Hemovac drain, including necessary treatments or interventions. A complaint submitted to the state health department indicated that the resident was later found to be not alert, babbling, lethargic, and altered during a post-operative visit, with lab results showing elevated white blood cells. The resident was subsequently sent to the emergency room and admitted to the hospital for further care. During interviews, facility nursing leadership acknowledged the omission of instructions in the baseline care plan regarding the surgical wound and Hemovac drain.
Failure to Monitor and Document Hemovac Drain Output per Professional Standards
Penalty
Summary
The facility failed to ensure that services provided met professional standards of quality in the care of a resident with a Hemovac drain following spinal surgery. Upon admission, documentation noted the presence of a surgical dressing and Hemovac drain with serosanguineous drainage, but there was no evidence that the output from the drain was measured or recorded according to facility policy, which requires emptying and measuring every 4 to 8 hours. Review of the resident's medical record revealed a lack of physician orders for monitoring, emptying, or documenting the Hemovac drain's function and output during the resident's stay. Staff interviews confirmed that there was no documentation or recollection of orders related to the drain, and the Assistant Director of Nursing and Director of Nursing were unable to provide evidence of required monitoring or orders for the drain during the relevant period. Further, during a follow-up appointment, the facility was unable to provide documentation of the Hemovac drain's output to the surgeon's physician assistant, who expected at least twice-daily monitoring and documentation. The facility physician also stated that standard practice includes having orders to monitor drainage, ensure proper function, and observe for infection. The lack of documentation and physician orders for the Hemovac drain's management, as well as the absence of output monitoring, constituted a failure to meet professional standards of quality for this resident.
Lack of Nurse Competency for Hemovac Drain Care
Penalty
Summary
The facility failed to ensure that nursing staff possessed the appropriate competencies and skill sets to provide care for residents with specific needs, as required by the facility assessment. Record review showed that the facility's resident population may include individuals with surgical wounds, and that nurse competencies should be completed during orientation, annually, and as dictated by resident care needs. Despite this, two LPNs who cared for a resident with a Hemovac drain following spinal fusion surgery reported not receiving any training specific to Hemovac drain care prior to providing care. The facility's policy on surgical wound treatment outlines the importance of proper management of closed-wound drains, including Hemovac drains, but the required competencies were not provided to the nursing staff. Interviews with the LPNs and the Director of Nursing Services confirmed that the facility did not provide education or competencies related to Hemovac drain care for any nursing staff. Documentation showed that a resident was admitted with a surgical wound and Hemovac drain, and staff were responsible for the care of this device without having received the necessary training. This lack of training and competency assessment was identified for 2 of 5 staff reviewed, resulting in a failure to ensure resident safety and the maintenance of the highest practicable well-being as required by regulation.
Failure to Implement Enhanced Barrier Precautions
Penalty
Summary
The facility failed to maintain an effective infection prevention and control program, specifically regarding Enhanced Barrier Precautions (EBP) for a resident with a wound requiring dressing. The resident, admitted in July 2024, had a wound on the coccyx that required various treatments from October to December 2024. Despite the presence of signage indicating the need for gown and glove use during high-contact care activities, staff members were observed not adhering to these precautions. On December 10, 2024, Nursing Assistants and an LPN were seen assisting the resident without wearing the required protective gear, despite the posted instructions. Interviews with staff revealed a lack of understanding and adherence to the EBP policy. Staff acknowledged the signage but failed to comply with the requirements during care activities. The Infection Preventionist and other nursing leaders were unable to provide evidence that the facility consistently followed EBP protocols as per their policy. The deficiency was highlighted by the absence of EBP implementation for the resident, who had a wound requiring a dressing since October 29, 2024, but was not placed on EBP until December 10, 2024.
What surveyors are citing around you — mapped
All 10 risk areas, ranked with evidence
Repeat citations, what's rising near you, and quality measures — ranked so department heads know exactly where to look first.
Illustrative
What surveyors actually found near you
We read the 637 citations issued within 25 miles in the last 12 months — including the 22 immediate-jeopardy cases — and tell you exactly what happened, in plain English, matched to your record.
Resident with a documented fall history left unattended on the patio; found on the ground with a hip fracture.
Walk-in cooler logs missing for 12 days; expired supplements in the medication room fridge.
Illustrative
A prioritized, do-first checklist
Every risk area becomes concrete audit steps drawn from real citations at facilities like yours — run them this week, before your window opens.
Illustrative
Risk indicators are statistical estimates from public CMS data — not predictions, findings, or compliance advice.
Nursing homes near Johnston
How nearby facilities compare on the same public inspection record.
| Facility | Distance | Overall rating | Citations, 12 mo | Serious (J–L) |
|---|---|---|---|---|
| Lincolnwood Rehabilitation And Healthcare Center | 2.1 mi | ★★★★★ | 9 | 0 |
| Golden Crest Nursing Centre | 2.2 mi | ★★★★★ | 8 | 0 |
| Briarcliffe Manor | 2.2 mi | ★★★★★ | 0 | 0 |
| Morgan Health Center | 2.4 mi | ★★★★★ | 3 | 1 |
| Elmhurst Rehabilitation And Healthcare Center | 2.5 mi | ★★★★★ | 10 | 1 |
Every risk area ranked, a do-first checklist, and your local survey patterns
Built specifically for Cherry Hill Manor.
100% money-back within 48 hours.
Trusted data, never guesswork. Every citation, penalty, rating and Plan of Correction on this page is sourced from public CMS records (latest release July 2026) and official state health department websites.