Inspired by Drive BTUC-8131M-BBRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383974613), received between Sep 13, 2022 and Sep 13, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (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.

• InjurySep 13, 2022Patient Device Interaction Problem; Patient Device Interaction Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BATH TRANSFER SYSTEM BY AN END USER, WHO REPORTED THAT WHILE HE WAS SEATED ON THE SYSTEM AND BEING ROLLED ACROSS A WOOD FLOOR BY HIS CAREGIVER, "THE WHEELS ON THE TRANSFER BASE LOCKED UP AND [WOULD] NOT ROLL," WHICH CAUSED HIM TO BE RUN INTO A WALL. HE WAS TAKEN TO THE ER WHERE HIS LEFT LEG WAS X-RAYED, AND WAS RELEASED THE SAME DAY. THE 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: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 15411636 ↗