Inadequate supervision of a high-elopement-risk resident
Summary
The facility failed to ensure that a resident with severe cognitive impairment, a known history of wandering, and a high elopement risk was appropriately supervised and monitored for safety. The resident’s record showed diagnoses including delirium due to a known physiological condition, hypertension, and bipolar disorder. The most recent MDS reflected a BIMS score of 5 out of 15, indicating severely impaired cognition, and the care plan identified the resident as having potential for wandering related to dementia and being at risk for elopement/wandering due to disorientation to place and impaired safety awareness. The resident’s elopement risk evaluation identified the resident as high risk for elopement and included use of a wander guard as needed. The February 2026 eTAR included orders for a wander guard bracelet on the right ankle with every-shift checks for function and placement. During interviews, multiple staff members described checking the bracelet by bringing the resident near the elevator or door to see whether the alarm activated, rather than using the transmitter tester described in the manufacturer’s user guide. The LPN, RN, RN/UM, CNA, ADON, DON, and LNHA each described the resident being taken near the elevator or door as the method used to check function. The manufacturer’s user guide stated that the transmitter should be tested using the transmitter tester and specifically noted, “Never take a resident to a door to test their transmitter.” The facility’s own Wander Guard policy also stated that daily every-shift testing was required and described the elevator alarm system, with nearby personnel to redirect the resident if the alarm sounded or the doors held in place. The surveyor observed the resident asleep in bed, and later, while the RN showed the wander guard bracelet on the resident’s ankle, the resident stated that they wanted to get out of here. The facility’s staff were inconsistent about the existence and use of a testing device, with some stating they were unaware of one and the MD later showing the surveyor the testing device in a drawer in the third-floor RN/UM office.
Penalty
Resources
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