DRIVEMEDICAL 369352Recalls & reported problems
Drive Devilbiss Healthcare · Bath SafetyGrab Bars Product Description: Grab Bar, Suction Cup,12",1EA,3/CS · Class 1
All models of DRIVEMEDICAL (111)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 50311917171307), received between Dec 23, 2020 and Mar 16, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated1
- Unintended Movement1
Patient problems
- Fall2
- Bone Fracture(s)1
- Head Injury1
- Vertigo1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 16, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A GRAB BAR BY AN END USER, WHO STATED THAT THE GRAB BAR "CAME LOOSE, AND HE FELL AND HIT THE LEFT SIDE OF HIS FACE ON THE SHOWER WALL." THE END USER REPORTEDLY WENT TO THE DOCTOR WHERE X-RAYS AND A SCAN WERE COMPLETED AND WERE NEGATIVE, HOWEVER THE END USER WAS REPORTEDLY ADVISED TO GO TO A NEUROLOGIST FOR A MORE DETAILED SCAN AS HE IS STARTING TO HAVE SYMPTOMS OF VERTIGO. 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; Head Injury; Vertigo
MAUDE report 16555415 ↗InjuryDec 23, 2020Unintended Movement; Unintended Movement
(B)(6) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A GRAB BAR. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. WE ARE FILING THIS REPORT TO BE TIMELY AND WILL SUBMIT A FOLLOW UP REPORT WHEN WE ACQUIRE ADDITIONAL DATA. THE END-USER FELL IN THE SHOWER WHEN THE GRAB BAR ALLEGEDLY MALFUNCTIONED. SHE SUFFERED A DISPLACED FRACTURE OF THE RIGHT FEMUR WHICH REQUIRED SURGERY.
Patient problems: Bone Fracture(s); Fall
MAUDE report 11069185 ↗
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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