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Handicare 323101Recalls & reported problems

Handicare USA, Inc. · C450 Manual Traverse - Quick Curve · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810045510453), received between Jul 26, 2023 and Jul 26, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Component Misassembled” (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

  • Component Misassembled1
  • Component Missing1

Patient problems

  • Abrasion1

Recent adverse event reports

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

  • InjuryJul 26, 2023Component Missing; Component Misassembled; Component Missing; Component Misassembled

    MOTOR CAME OUT OF THE END OF THE TRACK WHEN THE CARE AID WAS RETURNING THE MOTOR TO THE DOCKING STATION. THE MOTOR HIT THE CARE AID CAUSING BRUISING ON THE BACK OF RIGHT HAND AND KNEE, NO HOSPITALIZATION. EMPLOYEE PUT ICE ON THE AREA AND WAS ABLE TO KEEP WORKING FOR HER ENTIRE SHIFT. UPON INSPECTION OF THE TRACK, THERE WERE NO SAFETY PINS INSTALLED.

    Patient problems: Abrasion

    MAUDE report 17402284 ↗

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.