DRIVE FLSCALERecalls & reported problems
Drive Devilbiss Healthcare · Patient Room Lifts Product Description Patient Lift Scale 660lbs capacity · 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 00822383002026), received between Aug 4, 2026 and Aug 4, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Mechanical 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.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 4, 2026Mechanical Problem
Drive Medical was notified of an incident involving a patient lift scale by the device provider who reported that the patient lift scale broke while in use and the end user fell resulting in multiple fractures. As part of its complaint review and evaluation process, Drive Medical will also notify the manufacturer of the product about this complaint.
Patient problems: Bone Fracture(s)
MAUDE report 50127279 ↗
Other SCALE, PATIENT devices
- Welch Allyn, Inc. 901110Welch Allyn, Inc. · SCALE, PATIENT3 reports
- Medline MDSMELSCALEMedline Industries, Inc. · SCALE, PATIENT2 reports
- Welch Allyn, Inc. 901110Welch Allyn, Inc. · SCALE, PATIENT1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.