Drive 12025KD-1Recalls & reported problems
Drive Devilbiss Healthcare · Transfer Bench, Heavy Duty, KD, 1/cs · Class 1
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 00822383227573), received between Nov 29, 2021 and Nov 29, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Collapse” (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
- Collapse1
Patient problems
- Fall1
- Head Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 29, 2021Collapse; Collapse
(B)(6) HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A BATH BENCH. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. WE WILL SUBMIT A FOLLOW-UP WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE. WHILE IN USE THE BACK LEG FOLDED. THE END USER FELL AND HIT HIS HEAD. HE WENT TO THE EMERGENCY ROOM FOR TREATMENT. NO ADDITIONAL DATA IS AVAILABLE AT THIS TIME.
Patient problems: Fall; Head Injury
MAUDE report 12881844 ↗
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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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