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DRIVEMEDICAL 13244Recalls & reported problems

Drive Devilbiss Healthcare · Patient RoomLifts Product Description: Bariatric Lift,Elect,Homecare Style,1/cs · 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 00822383118086), received between Jul 11, 2022 and Jul 11, 2022 — classified as 1 injury.

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

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryJul 11, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A LIFT MODEL NUMBER 13244 IN WHICH THE PATIENT WAS REPORTEDLY SERIOUSLY INJURED. NO DETAILS ARE AVAILABLE REGARDING THE INCIDENT, PATIENT, AND TREATMENT. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT TO EVALUATE IT.

    Patient problems: Insufficient Information

    MAUDE report 14977903 ↗

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.