Drive 10244-4Recalls & reported problems
Drive Devilbiss Healthcare · Walker,Steel, Adult 2Button 5inWhls,4/CS · Class 1
Data updated Oct 16, 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 50822383515620), received between Jun 4, 2020 and May 7, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Material Twisted/Bent” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Twisted/Bent1
- Use of Device Problem1
Patient problems
- Bone Fracture(s)1
- Fall1
- Laceration(s)1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 7, 2026Use of Device Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WALKER BY THE END USER, WHO REPORTED THAT WHILE USING THE WALKER, THE WALKER HIT A CRACK AND STOPPED ABRUPTLY, CAUSING HER TO FALL OVER THE TOP OF THE WALKER AND SUSTAIN A FRACTURE IN THE TIP OF HER TIBIA. THERE WAS NO SPECIFIED DEFECT IN OR MALFUNCTION OF THE DEVICE. PRODUCT LABELING STATES,"BE AWARE OF THE FOLLOWING, GAPS IN THE FLOOR." AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.
Patient problems: Bone Fracture(s)
MAUDE report 25110559 ↗InjuryJun 4, 2020Material Twisted/Bent; Material Twisted/Bent
DRIVE DEILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. WE HAVE RECEIVED PHOTOS OF THE DAMAGED DEVICE. END-USER IS NOT RETURNING THE DEVICE FOR EVALUATION. SPOUSE REPORTED THAT WALKER DISPENSED TO PATIENT FAILED AS ONE OF THE LEGS ON THE WALKER BENT;. PATIENT FELL HITTING HIS HEAD RESULTING IN BLEEDING THE FOLLOWING DATA IS FROM NOTES FROM PHYSICAL THERAPY ASSOCIATE WITH ASSESSMENT INITIAL VISIT ON WHEN WALKER RECEIVED. PATIENT IS HOMEBOUND WITH POOR ENDURANCE AND SOB WITH MINIMAL ACTIVITY, GAIT IS LIMITED TO HOUSEHOLD DISTANCES. PATIENT IDENTIFIED AS HIGH RISK TO FALL ENVIRONMENT DESCRIBED AS CLUTTERED, PETS POORLY CONTROLLED, SLIP HAZARDS PRESENT. PATIENT VERY UNSAFE WITH ROLLING WALKER.
Patient problems: Fall; Laceration(s)
MAUDE report 10119546 ↗
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
- DRIVEMEDICAL 795BDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive 10257RD-1Drive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R728BLDrive 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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