DRIVEMEDICAL 13245Recalls & reported problems
Drive Devilbiss Healthcare · Patient RoomLifts Product Description: Bariatric Electric Patient Lift,1/cs · Class 1
All models of DRIVEMEDICAL (111)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00822383117898), received between Feb 26, 2020 and Feb 26, 2020.
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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
Feb 26, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A S PATIENT LIFT. THIS REPORT IS IN RESPONSE TO MW5091616. WE ARE CORRECTING INACCURATE DATA IN THE REPORT. PATIENT WAS IN A LIFT SLING WHEN THEY MOVED TO THE RIGHT AND FELL. HE WAS LETHARGIC. HE WAS TAKEN TO THE EMERGENCY ROOM FOR TESTS THAT WERE NEGATIVE. NO INJURY AS A RESULT OF THE FALL. THE LIFT IS 6 YEARS OLD. THERE IS NO DEFICIENCY IN THE LIFT OR THE SLING. THE MW REPORT NOTES SERIOUS INJURY WHICH IS INACCURATE.
Patient problems: Fall
MAUDE report 9759554 ↗
Other LIFT, PATIENT, NON-AC-POWERED devices
- MEDLINE MDS88200DMedline Industries, Inc. · Lift, patient, non-ac-powered108 reports
- Medline MDS600ELBMedline Industries, Inc. · Lift, patient, non-ac-powered82 reports
- Likorall™ overhead lift 3123001Liko AB · Lift, patient, non-ac-powered1 recall1 death32 reports
- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Likorall™ overhead lift 3121001Liko AB · Lift, patient, non-ac-powered1 recall24 reports
- Likorall™ overhead lift 3124050Liko AB · Lift, patient, non-ac-powered1 recall18 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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