DRIVEMEDICAL EQKW100Recalls & reported problems
Drive Devilbiss Healthcare · Walkers, All TypesKnee Walkers Product Description: Equate Steerable Knee Walker, 1/EA · 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 00681131006880), received between Nov 19, 2020 and Nov 19, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Unintended Movement” (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
- Adverse Event Without Identified Device or Use Problem1
- Unintended Movement1
Patient problems
- Abrasion1
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 19, 2020Adverse Event Without Identified Device or Use Problem; Unintended Movement; Adverse Event Without Identified Device or Use Problem; Unintended Movement
(B)(6) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. WE HAVE NOT RECEIVED THE UNIT FOR EVALUATION. WHEN WE EVALUATE THE UNIT WE WILL FILE A FOLLOW UP REPORT. THE DEVICE MOVED UNEXPECTEDLY WHILE IN USE IN THE DOCTOR'S OFFICE CAUSING THE END-USER TO FALL. THE USER REPORTS BRUISING OF HER RIGHT LEG WHICH CAUSED BLOOD CLOTS AND ARTHRITIS.
Patient problems: Abrasion; Fall
MAUDE report 10871384 ↗
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- Drive 10257RD-1Drive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- DRIVEMEDICAL 795BDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R726BKDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
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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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