DRIVEMEDICAL RTL12087Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383252841), received between Jul 25, 2019 and Nov 13, 2020 — 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. 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.

• InjuryNov 13, 2020Loose or Intermittent Connection; Loose or Intermittent Connection

  DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A TOILET SUPPORT RAIL. THE DEVICE HAS NOT BEEN RECEIVED FOR EVALUATION. WHEN THE EVALUATION RESULTS ARE AVAILABLE A FOLLOW-UP REPORT WILL BE FILED. WHILE USING THE DEVICE THE RIGHT ARM PIN CAME OUT. THE USER FELL DOWN INTO THE BATH TUB. THE PATIENT WAS HOSPITALIZED FOR THREE DAYS.

  Patient problems: Fall

  MAUDE report 10838639 ↗
• InjuryJul 25, 2019Break; Break

  (B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A BATH SAFETY DEVICE TOILET SUPPORT. THERE ARE NO PICTURES OF THE DEVICE. WE ARE NOT EXPECTING RETURN OF DEVICE. CONSUMER IS REQUESTING COMPENSATION. THE UNIT WAS RECEIVED AUGUST 2018. THE HANDLE BROKE ON THE LEFT SIDE AND CAUSED HER TO FALL. FIRE DEPARTMENT CALLED TO TAKE HER TO HOSPITAL WHERE SHE WAS DIAGNOSED WITH FRACTURED HIP AND PELVIS. OPTED OUT OF HIP REPLACEMENT AND HAD HIP REPAIRED. HOSPITALIZED FOR ALL OF (B)(6). REHAB AFTERWARDS. OCCUPATIONAL AND PHYSICAL THERAPISTS ASSISTED HER EVERY DAY ONCE SHE WAS HOME IN (B)(6).

  Patient problems: Hip Fracture

  MAUDE report 8829133 ↗