Drive 10200-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00822383117331), received between Jun 11, 2020 and Feb 6, 2026 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Material Twisted/Bent” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 6, 2026Mechanical Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WALKER BY THE END USER WHO STATED THAT WHILE USING THE DEVICE, THE DEVICE BEGAN TO MOVE AWAY UNEXPECTEDLY. THE END USER ATTEMPTED TO ENGAGE THE FOOT BRAKES; HOWEVER, THE BRAKES DID NOT STOP THE WALKER, AND THE USER SUBSEQUENTLY FELL. THE REPORTED INJURIES INCLUDED A FRACTURED HIP, WHICH REQUIRED SURGICAL INTERVENTION, AND A SHOULDER INJURY, WHICH IS BEING MANAGED THROUGH PRESCRIBED THERAPEUTIC EXERCISES. AS PART OF DRIVE DEVILBISS HEALTHCARE'S COMPLAINT REVIEW AND EVALUATION PROCESS, THE MANUFACTURER OF THE PRODUCT WILL ALSO BE NOTIFIED OF THIS COMPLAINT.

  Patient problems: Bone Fracture(s); Hip Fracture

  MAUDE report 24283105 ↗
• MalfunctionMay 30, 2023Material Twisted/Bent; Material Twisted/Bent

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A WALKER BY AND END USER'S WIFE, WHO STATED "HER HUSBAND FELL DOWN" WHILE USING THE WALKER. THE REPORTER STATED THAT THE WALKER'S LEG WAS BENT, BUT WAS UNSURE WHETHER THE LEG WAS BENT PRIOR TO THE FALL, OR AS A RESULT OF THE FALL. SHE CONFIRMED THAT HER HUSBAND DID NOT SUSTAIN ANY INJURIES, AND DID NOT SEEK ANY MEDICAL TREATMENT. DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

  Patient problems: Fall

  MAUDE report 17019119 ↗
• InjuryJun 11, 2020Material Twisted/Bent; Material Twisted/Bent

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. THIS REPORT IS FILED AS RESULT OF A REGRESSION ANALYSIS. END-USER WAS PRESCRIBED THE WALKER AFTER UNDERGOING SURGERY. SHE COULD NOT BEAR WEIGHT ON HER LEFT FOOT. SHE WAS "HOPPING" WITH THE WALKER AT NIGHT WHEN THE WALKER LEG BENT BACKWARDS SHE FELL FORWARDS AND HIT HER HEAD ON THE DRESSER. SHE WAS UNCONSCIOUS AND AWOKEN BY HER DAUGHTER.THE END-USER REFUSED TO GO TO THE HOSPITAL. SHE SUSTAINED A BLACK EYE. THE WALKER WAS REPLACED BY A CRUTCH AT THE BEEST OF HER DAUGHTER. AFTER THE SURGERY HER CARETAKER NOTED THAT THE PATIENT COULD NOT USE THE WALKER IN THE PROPER MANNER SINCE SHE COULD NOT BEAR WEIGHT ON HER LEFT FOOT. THE DEVICE WAS 3 DAYS OLD. ANALYSIS OF THE CAUSE OF THE DEVICE MALFUNCTION WAS DUE TO THE DEVICE NOT BEING USED AS INTENDED.

  Patient problems: Fall

  MAUDE report 10146388 ↗