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Handicare 323100Recalls & reported problems

Handicare USA, Inc. · C450 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 00810045510057), received between Jul 28, 2021 and Jul 28, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Installation-Related Problem” (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

Device problems

  • Installation-Related Problem1

Patient problems

  • Abrasion1
  • Bruise/Contusion1
  • Fall1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 28, 2021Installation-Related Problem; Installation-Related Problem

    A PATIENT WAS ABOUT TO BE TRANSPORTED WHEN THE CEILING TRACK AND LIFT FELL FROM THE CEILING. THE PATIENT FELL ONTO HIS BED AND RECEIVED TWO SCRATCHES AND A BRUISE.

    Patient problems: Abrasion; Bruise/Contusion; Fall

    MAUDE report 12241766 ↗

Other Lift, Patient, Non-Ac-Powered devices

All Lift, Patient, Non-Ac-Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.