Walmart EQKW200Recalls & reported problems
Drive Devilbiss Healthcare · Walkers, All Types Private Label Product Description Walmart Folding Knee Walker Selling Unit · Class 1
Data updated Oct 13, 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 00681131408592), received between Apr 24, 2025 and Apr 24, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Mechanical Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem1
Patient problems
- Damage to Ligament(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 24, 2025Mechanical Problem; Mechanical Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A KNEE WALKER BY THE END USER'S SPOUSE, WHO STATED THAT THE KNOB THAT SECURES THE HANDLEBAR HEIGHT IS TOO SHORT AND THAT IT CAME OUT OF THE HANDLEBAR WHILE SHE WAS USING IT CAUSING HER TO LOSE CONTROL OF THE STEERING. THE END USER FELL AND TORE LIGAMENTS IN HER LEFT ANKLE. A REVIEW OF THE COMPLAINT HISTORY FOR THIS PRODUCT REVEALS NO OTHER COMPLAINTS AND THIS APPEARS TO BE AN ISOLATED EVENT. 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: Damage to Ligament(s)
MAUDE report 21899374 ↗
Other WALKER, MECHANICAL devices
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- Drive 10257RD-1Drive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R726BKDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R728BLDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- DRIVEMEDICAL 795BDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive RTL10266Drive 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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