Drive 10210-4ASM (UDI 50822383226205)Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 50822383226205), received between Dec 17, 2019 and Feb 10, 2026 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Difficult to Open or Close” (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.

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 10, 2026Material Integrity Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WALKER BY THE END USER'S DAUGHTER, WHO REPORTED THAT THE WALKER BROKE DURING USE, CAUSING THE END USER TO FALL RESULTING IN BROKEN BONES IN HER FACE, WITH SWELLING AND FACIAL SCARRING. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Scar Tissue; Skull Fracture

  MAUDE report 24307718 ↗
• InjuryJan 29, 2020Material Fragmentation; Material Fragmentation

  DRIVE DEVIILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. THE DEVICE HAS NOT BEEN RECOVERED FOR EVALUATION. WHILE USING THE WALKER THE LEG BROKE OFF. THE END-USER FELL AND HIS HEAD REPORTEDLY WENT THROUGH A WALL. HE WENT TO THE EMERGENCY ROOM. HE IS SCHEDULED FOR A BRAIN SCAN THIS WEEK.

  Patient problems: Fall; Head Injury

  MAUDE report 9643480 ↗
• MalfunctionDec 17, 2019Difficult to Open or Close

  PATIENTS EXPERIENCING DIFFICULTIES OPENING AND CLOSING LEGS OF WALKERS.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9481058 ↗