DRIVEMEDICAL BRTL12606-ASTRecalls & reported problems
Drive Devilbiss Healthcare · Bath SafetyBenches/Stools Product Description: Shower Chair,Arms,SoapTrays,1/EA,RTL · Class 1
All models of DRIVEMEDICAL (111)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00822383927305), received between Aug 29, 2018 and Oct 31, 2022 — classified as 3 injuries.
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Collapse1
- Fracture1
- Material Integrity Problem1
Patient problems
- Fall3
- Bone Fracture(s)1
- Bruise/Contusion1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 31, 2022Material Integrity Problem; Material Integrity Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BATH STOOL BY AN END USER'S SISTER, WHO STATED THAT THE "SHOWER CHAIR COLLAPSED UNDER MY BROTHER WHILE IN SHOWER AND RESULTED IN BRUISING ACROSS CHEST, RIBS AND COCCYX AREA." THE END USER REPORTEDLY TOOK TYLENOL FOR PAIN BUT DID NOT SEEK FURTHER MEDICAL TREATMENT. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Fall
MAUDE report 15699888 ↗InjuryDec 10, 2019Fracture; Fracture
DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A BATH BENCH. THE END-USER IS UNWILLING TO RETURN THE DEVICE. WE WILL BE UNABLE TO EVALUATE FOR ROOT CAUSE. END-USER WAS SITTING ON THE DEVICE IN THE SHOWER. IT CRACKED AND SHE FELL. EMTS AND FIRE DEPARTMENT PERSONNEL HAD TO ASSIST HER IN GETTING UP. SHE DID NOT SEEK MEDICAL ATTENTION. SHE WAS SORE AND BRUISED AFTER INCIDENT. END-USER HIT HER HEAD ON THE SHOWER. SHE HAD A BUMP ON HER HEAD. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION DUE TO THE HEAD INJURY.
Patient problems: Bruise/Contusion; Fall
MAUDE report 9447907 ↗InjuryAug 29, 2018Collapse; Collapse
(B)(6) HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A BATH CHAIR. WE DO NOT HAVE THE DEVICE FOR EVALUATION BUT WILL CONTINUE TO ATTEMPT TO ACQUIRE IT. THE END-USER WAS IN THE SHOWER UTILIZING THE CHAIR. THE UNIT COLLAPSED CAUSING HIM TO FALL. THE USER FELL INJURING HIS SHOULDERS, NECK AND BACK. HE DID GO TO THE E.R WHERE THEY REFERRED HIM TO AN ORTHOPOD. THE DIAGNOSIS SHOWED FRACTURES IN BOTH OF HIS SHOULDERS AS WELL AS SOME TEARS.
Patient problems: Bone Fracture(s); Fall
MAUDE report 7827755 ↗
Other ADAPTOR, HYGIENE devices
- DRIVEMEDICAL RTL12505Drive Devilbiss Healthcare · ADAPTOR, HYGIENE19 reports
- 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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