DRIVEMEDICAL 146-11148-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00612479222069), received between Apr 12, 2023 and Apr 12, 2023 — classified as 2 injuries.

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

• InjuryApr 12, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY AN END USER'S ATTORNEY, WHO STATED THAT THE "RIGHT FRONT FORK AND CASTER FAILED, AND SHE FELL," REPORTEDLY RESULTING IN INJURIES REQUIRING SURGERY AND PHYSICAL THERAPY. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Fall

  MAUDE report 16725603 ↗
• InjuryApr 12, 2023Collapse; Collapse

  (B)(6) WAS NOTIFIED OF AN INCIDENT INVOLVING A BATH CHAIR BY AN END USER'S CAREGIVER, WHO STATED THAT THE "LEGS OF THE CHAIR COLLAPSED, AND THE END USER FELL AND HIT HER HEAD ON HER ROLLATOR." THE END USER DID NOT SEEK ANY MEDICAL ATTENTION. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Fall; Head Injury

  MAUDE report 16725254 ↗