Drive 10210-4ASM (UDI 00822383226200)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383226200), received between Mar 19, 2020 and Jan 29, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Defective Device” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJan 29, 2025Mechanical Problem; Mechanical Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WALKER BY THE END USER, WHO REPORTED THAT THE BACK RIGHT LEG BENT, CAUSING HER TO FALL AND SUSTAIN A FRACTURED HEEL AND BRUISING. INSPECTION OF THE DEVICE CONFIRMED THAT THE LEG WAS BENT. 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: Bone Fracture(s)

  MAUDE report 21265674 ↗
• MalfunctionMar 19, 2020Defective Device

  UPON DEMONSTRATING ROLLING WALKER TO ISSUE TO PATIENT FOR HOME, NOTED TO BE DEFECTIVE REQUIRING EXCESSIVE FORCE TO CLOSE RIGHT- HAND SIDE. REPLACED WITH A NEW WALKER, WHICH FUNCTIONED APPROPRIATELY.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9853172 ↗