DRIVEMEDICAL 12044Recalls & reported problems
Drive Devilbiss Healthcare · Bath SafetyGrab Bars Product Description: Tub Rail,16 1/2"Plastic,1/bx, 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 00822383119540), received between Nov 27, 2019 and Nov 27, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Bruise/Contusion1
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 27, 2019Break; Break
DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A TUB RAIL. THE UNIT HAS NOT BEEN RETURNED FOR EVALUATION. THE END-USER FELL WHEN THE UNIT BROKE AS HE STOOD UP IN THE TUB. HE STATES HE INJURED HIS WRIST, RIGHT KNEE AND FINGERS ON EACH HAND. HE WENT TO THE ER.
Patient problems: Bruise/Contusion; Fall
MAUDE report 9385082 ↗
Other ADAPTOR, HYGIENE devices
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- Drive RTL12202KDRDrive Devilbiss Healthcare · ADAPTOR, HYGIENE11 reports
- 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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