Drive 11148N-4Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 50822383222030), received between Oct 4, 2019 and May 27, 2026 — classified as 2 injuries.

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

• InjuryMay 27, 2026Break

  DRIVE MEDICAL WAS NOTIFIED OF AN INCIDENT INVOLVING A COMMODE BY A LETTER FROM AN ATTORNEY WHO REPORTED THE LEG OF THE COMMODE GAVE OUT CAUSING THE COMMODE TO COLLAPSE. THE END USER FELL AND FRACTURED THEIR RIGHT HEEL BONE. DRIVE MEDICAL IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO INSPECT THE DEVICE. AN UPDATE WILL BE FILED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Bone Fracture(s)

  MAUDE report 25303829 ↗
• InjuryOct 4, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  (B)(6) HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A COMMODE. WE ARE STILL AWAITING RETURN OF THE DEVICE FOR EVALUATION. ACCORDING TO DAUGHTER, HER MOTHER FELL WHILE USING THE DEVICE IN THE EVENING. SHE HAD A LACERATION IN THE BACK OF HER HEAD FROM THE FALL. THEY TOOK HER TO THE HOSPITAL TO HAVE HER CHECKED OUT. PER DAUGHTER, THE FRONT RIGHT LEG ON THE COMMODE IS LONGER THAN THE LEFT LEG.

  Patient problems: Laceration(s)

  MAUDE report 9158354 ↗