Drive TR18Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383132044), received between Feb 6, 2026 and Feb 6, 2026 — 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. How this data works · Data updated Oct 13, 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.

• InjuryFeb 6, 2026Mechanical Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY THE END USER'S DAUGHTER WHO STATED THE WHEEL LOCKS DID NOT ENGAGE, AND THE WHEELCHAIR MOVED AS THE END USER ATTEMPTED TO SIT DOWN. THE END USER SUBSEQUENTLY FELL, SUSTAINING A FEMUR FRACTURE. SURGICAL INTERVENTION WAS REQUIRED, AND THE INDIVIDUAL IS CURRENTLY RECEIVING CONTINUED CARE IN A REHABILITATION FACILITY. THE PRODUCT LABELING FOR THIS WHEELCHAIR INSTRUCTS USERS TO ENGAGE THE DUAL WHEEL LOCKS AGAINST THE REAR TIRES AND TO ENSURE THE FRONT CASTERS ARE POSITIONED FORWARD BEFORE ENTERING OR EXITING THE CHAIR. 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: Limb Fracture

  MAUDE report 24283104 ↗