APEX HOY-ELEVATE-SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00810055880089), received between Apr 29, 2025 and Apr 29, 2025 — classified as 2 injuries.

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryApr 29, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT ONE RESIDENT HAD SKIN TEARS ON HIS THUMBS DUE TO THE NEW HANDLE LOCATION ON THE ELEVATE LIFT. THIS NOT A NEW HANDLE POSITION OR LOCATION, THIS IS A NEWER VERSION OF THE HANDLE THAT THE CUSTOMER HAS HAD IN THE PAST. COMPLAINT # (B)(4) WAS ENTERED INTO OUR SYSTEM.

  Patient problems: Skin Tears

  MAUDE report 21931896 ↗
• InjuryApr 29, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT ONE RESIDENT HAD TWO FALLS FROM A NEW SIT TO STAND DUE TO HOW THE HANDLES ARE ON THE OUTSIDE OF THE BARS, AND AN ELDERLY, WEAK, PERSON IS FORCED TO KEEP ARMS TOO FAR TO THE SIDES AWAY FROM THE BODY, WHICH TAKES A LOT OF UPPER BODY STRENGTH. COMPLAINT # (B)(4) WAS ENTERED INTO OUR SYSTEM.

  Patient problems: Fall

  MAUDE report 21931895 ↗