Drive 15033BV-FRRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383211732), received between Jul 16, 2025 and Jul 16, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Temperature 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.

• MalfunctionJul 16, 2025Temperature Problem; Temperature Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING AN ELECTRIC BED BY THE CARETAKER WHO STATED THAT A FIRE OCCURRED UNDERNEATH THE BED DUE TO (REMOTE) WIRES SHORTING OUT. EXAMINATION OF PROVIDED PICTURES, HOWEVER, SHOWS NO EVIDENCE OF A FIRE. THERE WAS NO REPORT OR EVIDENCE OF ILLNESS OR SERIOUS INJURY ASSOCIATED WITH THE COMPLAINT. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22522089 ↗