Failure to obtain assessment and consent for restrictive safety devices
Summary
The facility failed to ensure that safety devices did not restrict residents’ ability to move and failed to have resident or representative consent for restrictive safety devices for 3 of 4 sampled residents reviewed for physical restraints. The deficiency involved Resident 51, Resident 66, and Resident 105, and surveyors identified the issue through observation, interview, and record review. Resident 51 was admitted with hospice care, depression, anxiety, and vascular dementia, was dependent on staff for ADLs, and was not able to communicate needs. The resident had a very low body weight and was observed multiple times in bed with half side rails raised on both sides while lying in a fetal or curled position, including during meals and while watching TV. The record showed a Device and Bed Rail/Bed Enabler Evaluation and consent for bilateral grab/assist/mobility bars, and the care plan listed bilateral grab bars for bed mobility, but staff could not find documentation to explain the use of half side rails. The RN/UM stated the process required therapy evaluation, consent, and assessment, and the DON stated any device that could be a potential restraint should have assessment, consent, and periodic reassessment. Resident 66 was admitted with repeated falls, diabetes, and dementia and was able to make needs known. The MDS showed the resident could independently wheel 150 feet in a wheelchair, but observation showed an anti-rollback device attached to both wheelchair wheels, preventing backward movement and causing the resident frustration. The EHR contained no order or consent for the device. Staff stated the device had been installed after a fall, that the resident could not self-propel backward, and that the resident would attempt to stand instead; the OT and DOR confirmed the resident was restrained from propelling backward and had not been assessed after the device was installed. Staff also stated the device was installed incorrectly. Resident 105 was admitted with dementia, unsteadiness on feet, and cognitive communication deficit. Observation showed a wander guard wrist band securely fastened to the left wrist. The EHR had no provider order, no wander guard assessment, no informed consent, and the quarterly MDS indicated a wander/elopement alarm was not used. The RN/UM stated the resident had an elopement risk evaluation for exit seeking, but it did not include an assessment for a wander guard, and staff could not locate the required order, assessment, consent, or documentation showing function and placement monitoring. The DON stated they were not aware those documents were missing and that they should have been in place.
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