DRIVEMEDICAL 10247-4Recalls & reported problems
Drive Devilbiss Healthcare · Walkers, All TypesJunior Product Description: Walker,Steel, Junior 2Button 5" Whs,4/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 50822383537257), received between Jul 19, 2022 and Sep 24, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Use of Device Problem” (2 reports).
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
- Use of Device Problem2
Patient problems
- Fall2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 24, 2022Use of Device Problem; Use of Device Problem
DRIVE DEVILBISS HEALTHCARE RECEIVED A COMPLAINT INVOLVING A WALKER FROM AN END USER, WHO REPORTED THAT WHILE USING THE WALKER, IT "SLID," CAUSING HER TO FALL. THE END USER STATED THAT "WITH ALL THE NARCOTICS IN HER BODY, [SHE] SHOULDN'T HAVE TO WORRY ABOUT THE SURFACES [SHE] WALKS ON." SHE STATED THAT TO HER KNOWLEDGE "NOTHING ON THE UNIT IS BROKEN BUT LEFT A SKID MARK ON HER FLOOR." AS A RESULT OF THE FALL, SHE HIT THE LEFT SIDE OF HER HEAD AND "RUPTURED HER EAR." DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT TO EVALUATE IT.
Patient problems: Fall
MAUDE report 15476886 ↗InjuryJul 19, 2022Use of Device Problem; Use of Device Problem
(B)(6) HEALTHCARE RECEIVED A COMPLAINT INVOLVING A WALKER FROM AN END USER, WHO REPORTED THAT WHILE USING THE WALKER, IT "SLID," CAUSING HER TO FALL. THE END USER STATED THAT "WITH ALL THE NARCOTICS IN HER BODY, [SHE] SHOULDN'T HAVE TO WORRY ABOUT THE SURFACES [SHE] WALKS ON." SHE STATED THAT TO HER KNOWLEDGE "NOTHING ON THE UNIT IS BROKEN BUT LEFT A SKID MARK ON HER FLOOR." AS A RESULT OF THE FALL, SHE HIT THE LEFT SIDE OF HER HEAD AND "RUPTURED HER EAR." DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT TO EVALUATE IT.
Patient problems: Fall
MAUDE report 15057719 ↗
Other WALKER, MECHANICAL devices
- Drive 10257BL-1Drive Devilbiss Healthcare · WALKER, MECHANICAL13 reports
- Drive R726RDDrive Devilbiss Healthcare · WALKER, MECHANICAL1 death10 reports
- Drive 790Drive Devilbiss Healthcare · WALKER, MECHANICAL10 reports
- Drive R728BLDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive 10257RD-1Drive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- DRIVEMEDICAL 795BDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R726BKDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive 10215BL-1Drive Devilbiss Healthcare · WALKER, MECHANICAL8 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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