Drive 15005LRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383563329), received between Dec 10, 2019 and Dec 10, 2019 — classified as 1 death.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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.

• DeathDec 10, 2019Use of Device Problem; Improper or Incorrect Procedure or Method; Use of Device Problem; Improper or Incorrect Procedure or Method

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A BED. THE SERVICE PROVIDER DELIVERED THE UNIT WITHOUT THE COMPONENT THAT ELEVATED THE HEAD. THE UNIT WAS INSTALLED INCOMPLETELY. THE FIRST UNIT PROVIDED IN HOSPITAL WAS A BED THAT WAS TOO SHORT. THIS UNIT WAS REPLACED ON (B)(6) 2019 WITH AN INCOMPLETE BED THAT WAS MISSING THE PART THAT ELEVATED THE HEAD OF BED. THE MISSING PIECE WAS SCHEDULED TO ARRIVE THAT NIGHT BUT WAS DELIVERED ON THE (B)(6). THE PATIENT WAS SUFFERING FROM UPPER RESPIRATORY CONGESTION. THIS CONDITION WAS FURTHER AGGRAVATED SINCE THE BED WAS NOT ELEVATED. THE PATIENT COULD NOT BREATHE AND DIED OF HIS OWN SECRETIONS ON THE NIGHT OF (B)(6). THE DIAGNOSIS OF HIS DEATH WAS RESPIRATORY DISTRESS.

  Patient problems: Death

  MAUDE report 9448482 ↗