Inspired by Drive BTUF-8130M-BBRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383974552), received between May 1, 2023 and May 1, 2023 — classified as 1 injury.

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

• InjuryMay 1, 2023Unintended Movement; Unintended Movement

  INOVO WAS NOTIFIED OF A COMPLAINT INVOLVING A BATH TRANSFER BENCH BY AN END USER'S MOTHER, WHO STATED "THE TUB BASE LEG THAT TELESCOPES WENT IN, GETTING SHORTER [AND] CAUSING MY SON TO FALL IN THE TUB." THERE WAS NO REPORT OR EVIDENCE OF ILLNESS, INJURY OR MEDICAL TREATMENT ASSOCIATED WITH THE COMPLAINT. THE END USER'S MOTHER STATED SHE WILL NOT BE RETURNING THE PRODUCT FOR INVESTIGATION. INOVO WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

  Patient problems: Fall

  MAUDE report 16844024 ↗