APEX HOY-ELEVATEWSC-SRecalls & reported problems
Joerns Healthcare, LLC · HOY-ELEVATE W/ SCALE AND SMART MONITOR · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810055880096), received between Aug 28, 2025 and Aug 28, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 28, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT RESIDENT WAS BEING MOVED FROM TOILET TO WHEELCHAIR VIA JOERNS SIT TO STAND DEVICE. DURING THE TRANSFER THE SIT STAND DEVICE FAILED CAUSING THE RESIDENT AND HER LNA TO END UP ON THE FLOOR. COMPLAINT #(B)(4) WAS ENTERED INTO OUR SYSTEM.
Patient problems: Insufficient Information
MAUDE report 22912220 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.