DRIVEMEDICAL 146-R726RDRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00612479223097), received between Jun 3, 2020 and Jun 3, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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.

• InjuryJun 3, 2020Fracture; Fracture

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. THE UNIT WAS NOT RETURNED FOR EVALUATION DUE TO COVID-19. WE RECEIVED IMAGES BUT NO EVALUATION REPORT FROM THE SERVICE PROVIDER. WE WILL FILE A FOLLOW UP IF NEW INFORMATION IS AVAILABLE. SERVICE PROVIDER'S REFERENCE NUMBER IS (B)(4). END-USER SAT ON THE DEVICE AND THE WHEEL CAME OFF. HE FELL TO THE GROUND AND HURT HIS HEAD, SHOULDER AND MOUTH. HIS DENTURES WERE DAMAGED REQUIRING DENTAL WORK. THE SERIAL NUMBER WAS RUBBED OFF OF THE UNIT FROM USE. SERVICE PROVIDER HAS NO ADDITIONAL INFORMATION.

  Patient problems: Fall; Neck Pain

  MAUDE report 10114038 ↗