DRIVEMEDICAL 13242Recalls & reported problems
Drive Devilbiss Healthcare · Patient RoomLifts Product Description: Electric Patient Lift w/Rem.Back,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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383125633), received between Jul 21, 2021 and Jul 21, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Component Missing” (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 18, 2026.
Most reported problems
Device problems
- Component Missing1
- Material Deformation1
Patient problems
- Fall1
- Hip Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 21, 2021Component Missing; Material Deformation; Component Missing; Material Deformation
DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS AN ELECTRONIC PATIENT LIFT. WE ARE AWAITING RETURN OF THE DEVICE FOR EVALUATION. WE HAVE RECEIVED PHOTOS OF THE DEVICE. WHEN ADDITIONAL INFORMATION IS RECEIVED A FOLLOW-UP SUBMISSION WILL BE TENDERED. THE FACILITY STATED THE PATIENT LIFT MALFUNCTIONED DURING OPERATION AND THE RESIDENT FELL. THE INCIDENT OCCURRED WHILE TRANSFERRING THE PATIENT FROM A BED TO A WHEELCHAIR. LIFT SHOWS SIGNS OF BENT METAL AND BOLT MISSING WHERE THE BOOM CONNECTS TO MAST. THE LIFT IS INOPERABLE. THE RESIDENT SUFFERED A HIP FRACTURE.. UNIT WAS USED FOR APPROXIMATELY 16 MONTHS. UNIT WAS USED BY MULTIPLE PATIENTS.
Patient problems: Fall; Hip Fracture
MAUDE report 12204874 ↗
Other LIFT, PATIENT, NON-AC-POWERED devices
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- 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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