Drive 15033BV-PKG-TRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383211848), received between Feb 27, 2023 and Feb 27, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Overheating of Device” (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.

• InjuryFeb 27, 2023Overheating of Device; Overheating of Device

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING AN ELECTRIC BED BY AN END USER, WHO STATED THAT "THEY WERE LAYING WITH THE REMOTE UNDER HER RIGHT HIP AND THE REMOTE CONTROL GOT HOT AND BURNED HER." THE END USER WENT TO A TELEHEALTH APPOINTMENT WHERE SHE REPORTEDLY TOLD THAT SHE WAS "ON THE VERGE OF A 1ST DEGREE BURN" AND PRESCRIBED OINTMENT FOR TREATMENT. 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: Burn(s)

  MAUDE report 16442735 ↗