DRIVEMEDICAL 741741Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00050428442548), received between Jun 20, 2020 and Jun 20, 2020 — classified as 1 injury.

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.

• InjuryJun 20, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ELEVATED TOILET SEAT. THIS REPORT IS BEING TENDERED IN AN OVERABUNDANCE OF CAUTION IN RESPONSE TO AN MDR REGRESSION ANALYSIS. WHEN THE END USER ATTACHED THE DEVICET ON THE TOILET THE BRACKETS KEPT COMING OFF. SHE CONTINUED TO USE IT AND FELL AND HIT HER HEAD. THE DEVICE WAS NT RETRIEVED FOR EVALUATION SINCE CONTACT INFORMATION WAS NOT PROVIDED BY THE CONTACT ENTITY.

  Patient problems: Fall; Head Injury

  MAUDE report 10177198 ↗