Drive KA2200-2GWPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383583853), received between Oct 10, 2024 and Oct 10, 2024 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryOct 10, 2024Mechanical Problem; Mechanical Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WALKER BY THE END USER'S MOTHER WHO STATED THAT THE END USER FELL FORWARD RECEIVING TWO STITCHES. THE DEVICE WAS RETURNED FOR EVALUATION. THE DEVICE'S REAR WHEEL WAS LOOSE AND MISALIGNED CAUSING THE WHEEL TO OPERATE AT AN ANGLE AND RUB AGAINST THE OVERRIDE BRACKET CAUSING DAMAGE TO THE BRACKET. WITH THE DAMAGE OVERRIDE BRACKET, THE OVERRIDE REAR BRAKE CAN EASILY DETACH FROM THE BRACKET AND FALL DOWN WHEN IT ENGAGES THE ONE DIRECTIONAL FEATURE. THIS CAN CAUSE THE WALKER TO BRAKE WHEN GOING IN ONE DIRECTION WHICH CAN CAUSE THE END USER TO FALL. PRODUCT LABELING INSTRUCTS THE USER TO REGULARLY INSPECT AND TIGHTEN NUTS AND BOLTS. DRIVE DEVILBISS HEALTHCARE CONCLUDES THE MISALIGNED WHEEL CAUSED INTERFERENCE, LIKELY DAMAGING THE BRACKET. 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: Laceration(s)

  MAUDE report 20421215 ↗