Handicare 324200Recalls & reported problems
Handicare USA, Inc. · A450 Manual Traverse · 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 00810045510996), received between May 3, 2024 and May 3, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Fell” (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
- Device Fell1
Patient problems
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 3, 2024Device Fell; Device Fell
CARE WORKER INJURED BY CARRY BAR FREE FALLING FROM OVERHEAD LIFT.
Patient problems: Bruise/Contusion
MAUDE report 19243926 ↗
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- Viking™ L mobile lift 2040044Liko AB · Lift, patient, non-ac-powered1 recall4 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.