Drive 15300Recalls & reported problems
Drive Devilbiss Healthcare · Bariatric Bed Pkg, 1pkg/cs · Class 2
Data updated Oct 13, 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 00822383180793), received between Apr 13, 2022 and Apr 13, 2022 — 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.
Most reported problems
Device problems
- Mechanical Problem1
Patient problems
- Ulcer1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 13, 2022Mechanical Problem; Mechanical Problem
ON (B)(6) 2022, (B)(6) HEALTHCARE WAS NOTIFIED OF AN INCIDENT REGARDING A FULL ELECTRIC BARIATRIC BED. THE END USER REPORTED THAT THE "HEAD WILL NOT GO UP AND THE BED WILL NOT COME DOWN WHEN RAISED," AND THAT SHE IS CURRENTLY IN THE HOSPITAL WITH BED SORES THAT SHE DEVELOPED WHEN THE BED WAS NOT WORKING PROPERLY. DRIVE HAS NOT RECEIVED ANY FURTHER INFORMATION REGARDING HOW THE BED'S FAILURE TO RAISE AND LOWER CAUSED THE END USER'S BED SORES. HOWEVER, DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT TO INSPECT IT.
Patient problems: Ulcer
MAUDE report 14105169 ↗
Other Bariatric bed devices
- Medline MDR107004Medline Industries, Inc. · Bariatric bed110 reports
- MV3 5900Stryker Corporation · Bariatric bed1 recall41 reports
- Medline FCEALTMAXXMedline Industries, Inc. · Bariatric bed84 reports
- Drive 15300BV-PKGDrive Devilbiss Healthcare · Bariatric bed2 reports
- Drive P503Drive Devilbiss Healthcare · Bariatric bed2 reports
- Synergy® Surface P6881CAPHill-Rom, Inc. · Bariatric bed2 reports
- Joerns Bari10AJoerns Healthcare, LLC · Bariatric Bed2 reports
- INVACARE® BAR600 BARIATRIC BED BAR600IVCInvacare Corporation · Bariatric Bed1 report
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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