DRIVEMEDICAL 12039Recalls & reported problems
Drive Devilbiss Healthcare · Bath SafetyGrab Bars Product Description: Tub Rail, 12"Plastic, 1/ea, RTL · 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 10822383102716), received between Apr 29, 2024 and Apr 29, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
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.
InjuryApr 29, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT BY THE END USER'S SPOUSE INVOLVING A TUB RAIL THAT REPORTEDLY CAME LOOSE WHILE THE END USER WAS USING IT TO GET OUT OF THE BATHTUB CAUSING HER TO FALL BACKWARDS. EMERGENCY ROOM X-RAYS REVEALED A BROKEN RIB. DRIVE DEVILBISS HEALTHCARE WILL UPDATE THIS REPORT SHOULD ANY ADDITIONAL INFORMATION BECOME AVAILABLE.
Patient problems: Bone Fracture(s)
MAUDE report 19205736 ↗
Other ADAPTOR, HYGIENE devices
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- Drive RTL12203KDRDrive Devilbiss Healthcare · ADAPTOR, HYGIENE9 reports
- Drive 12011KD-1Drive Devilbiss Healthcare · ADAPTOR, HYGIENE1 death9 reports
- DRIVEMEDICAL 12486Drive Devilbiss Healthcare · ADAPTOR, HYGIENE6 reports
- DMI 522-1702-1900D-M-S Holdings, Inc. · Adaptor, Hygiene5 reports
- Drive 11135-1Drive Devilbiss Healthcare · ADAPTOR, HYGIENE4 reports
- Aquasence 770-525Drive Devilbiss Healthcare · ADAPTOR, HYGIENE4 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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