Handicare 2000Recalls & reported problems
Handicare Accessibility Limited · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05056233700045), received between Apr 24, 2026 and May 22, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Failure to Align” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Align1
- Fracture1
- Vibration1
Patient problems
- Bruise/Contusion1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 22, 2026Fracture
END USER WAS RIDING THE STAIRLIFT UPWARD, WHEN THEY HEARD A POP. THEY SAFELY RODE TO THE NEAREST STOP AT THE BOTTOM AND IT WAS FOUND THAT THE RAIL HAD A SMALL BREAK. THEY RODE OVER THE WELD BREAK AND SAFELY EXITED THE STAIRLIFT WITHOUT ANY INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25255824 ↗InjuryApr 24, 2026Vibration; Failure to Align
END USER STATES THAT SEAT SWIVEL DID NOT WORK. END USER TRAVELLED UP STAIRS, ONCE AT THE LANDING THE SWIVEL MOTOR FAILED TO ENGAGE. END USER ATTEMPTED TO LEAVE THE LIFT IN A PANICKED STATE, UPON DISEMBARKING HIS LEGS GAVE WAY RESULTING IN HIM FALLING AGAINST THE WALL AND BEING UNABLE TO GET UP. SUSTAINED BRUISES.
Patient problems: Bruise/Contusion
MAUDE report 24982057 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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