DRIVEMEDICAL 990XRecalls & reported problems
Drive Devilbiss Healthcare · Walkers, All TypesKnee Walkers Product Description: All-Terrain Knee Walker, 1/CS · 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 00822383585192), received between Jul 17, 2019 and Jul 17, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Material Fragmentation” (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
- Material Fragmentation1
Patient problems
- Bone Fracture(s)1
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 17, 2019Material Fragmentation; Material Fragmentation
(B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A KNEE WALKER. WE HAVE NOT RECEIVED THE PRODUCT RETURN AT THIS TIME. IT IS WITH THE SERVICE PROVIDER WHO RENTED THIS DEVICE. CONSUMER RENTED THE DEVICE FOR USE ON HER TRIP ABROAD. SHE COULD NOT PUT WEIGHT ON HER FOOT WHILE IT HEALED. WHILE PACKING SHE PUSHED OFF WITH HER GOOD FOOT. THE KNEE WALKER STOPPED MOVING AS THE WHEELS WENT OUT FROM UNDERNEATH HER. THE TOP SNAPPED OFF THE DEVICE. THE USER FELL FORWARD AND HIT HER COLLARBONE. XRAYS WERE TAKEN BY A DOCTOR. SHE REPORTED THAT SHE HAD 2 FRACTURES OF HER RIGHT FOOT, A SPRAINED KNEE AND A BRUISED COLLARBONE. SHE IS LOOKING FOR COMPENSATION. .
Patient problems: Bone Fracture(s); Bruise/Contusion
MAUDE report 8800875 ↗
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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