Handicare 323117Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00810045510484), received between Jul 27, 2021 and Jan 9, 2026 — classified as 2 injuries, 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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryJan 9, 2026Unintended Movement

  WE HAD ONE OF OUR 625LB HANDICARE CEILING LIFTS THAT WAS HOLDING THE VET APPROXIMATELY 18 INCHES ABOVE A TOILET WHEN THE STRAP SUDDENLY DROPPED. THE STRAP IS INTACT BUT SOUNDS LIKE IT SLIPPED, DROPPING THE VET BACK ONTO THE TOILET. THE VET WAS TRANSPORTED TO THE HOSPITAL WITH A FRACTURE.

  Patient problems: Bone Fracture(s)

  MAUDE report 24022780 ↗
• MalfunctionAug 15, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  CAREGIVER STATED THAT WHILE TRANSFERRING THE PATIENT FROM THE BED TO THE WHEELCHAIR, THE LIFT DROPPED WHILE OVER THE WHEELCHAIR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22820642 ↗
• InjuryJul 27, 2021Use of Device Problem; Use of Device Problem

  PATIENT WAS BEING TRANSFERRED OUT OF AVERO MOTION BATH WHEN THE SHOULDER ATTACHMENT OF THE SLING RELEASED FROM THE BULL HORN CARRY BAR OF A C625 OVERHEAD LIFT. THE PATIENT FELL AND BROKE HIS HIP.

  Patient problems: Fall; Hip Fracture

  MAUDE report 12235037 ↗