Drive 12029-2Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50822383110597), received between Jul 11, 2022 and Jul 11, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

• InjuryJul 11, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BATH BENCH BY A DISTRIBUTOR, WHO REPORTED THAT "THE LEGS ARE NOT STURDY, AND THE PATIENT FELL OFF THE BENCH TWICE, LAST TIME HAD TO GO TO THE HOSPITAL." THE DEVICE WAS NOT RETURNED FOR EVALUATION, AND THE PATIENT DID NOT RESPOND TO ATTEMPTS AT CONTACT TO GATHER MORE INFORMATION.

  Patient problems: Fall

  MAUDE report 14980902 ↗