Drive 15030Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00822383111094), received between Sep 21, 2021 and Apr 3, 2026 — classified as 1 death, 4 injuries.

The most frequently reported specific device problem is “Device Slipped” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• DeathApr 3, 2026Insufficient Device Problem Information

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED BY ATTORNEY LETTER OF THE PRESENCE AND POTENTIAL INVOLVEMENT OF A SEMI-ELECTRIC BED IN A FIRE, AND THE END USER WAS INJURED AND SUBSEQUENTLY DIED AS THE RESULT OF A FIRE. DRIVE DEVILBISS HEALTHCARE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO INSPECT THE PRODUCT THROUGH THE ATTORNEY. AN UPDATE WILL BE FILED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Burn(s)

  MAUDE report 24781778 ↗
• InjuryJan 18, 2024Device Slipped; Device Slipped

  DRIVE DEVILBISS HEALTHCARE RECEIVED A LETTER FROM AN ATTORNEY REPRESENTING AN END USER, WHICH ALLEGED THAT A DELTA PRO BED "SLIPPED," CAUSING THE END USER TO FALL AND SUSTAIN SIGNIFICANT INJURIES. THE ATTORNEY DID NOT SPECIFY THE INJURIES IN THE LETTER. DRIVE IS CURRENTLY ATTEMPTING TO INSPECT THE PRODUCT IN COOPERATION WITH THE ATTORNEY. DRIVE WILL FILE AN UPDATE AS SOON AS ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Insufficient Information

  MAUDE report 18537950 ↗
• InjuryJun 8, 2023Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING AN ELECTRIC BED BY A HEALTHCARE PROVIDER, WHO STATED THAT THE END USER WAS "SLEEPING ON THE HAND CONTROL WHEN SHE FELT A SHOCK [AND] RECEIVED 3RD DEGREE BURN ON LEFT HIP," FOR WHICH SHE WAS TREATED WITH BANDAGES BY HER HOME HEALTH AIDES. SHE REPORTEDLY OBSERVED RUST ON TWO OF THE SCREWS ON THE HAND CONTROL, WHICH MAY INDICATE THAT THE HAND CONTROL WAS SOMEHOW EXPOSED TO MOISTURE AND COMPROMISED. 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 17087727 ↗
• InjuryMay 16, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT INVOLVING A BEDRAIL BY THE END USER'S SON, WHO REPORTED THAT HIS FATHER "HAS ALZHEIMER'S AND IS INJURING HIS ARMS BY PUTTING HIM THROUGH THE RAILS," AND THAT HE BELIEVES THE MANUFACTURER SHOULD "PROVIDE THE PADS TO KEEP THIS FROM HAPPENING." IT IS UNCLEAR WHAT PADS TO WHICH THE REPORTER REFERRED, AND THERE WAS NO FURTHER INFORMATION PROVIDED REGARDING THE SPECIFICS OR SEVERITY OF THE REPORTED INJURY. DRIVE IS CURRENTLY INVESTIGATING THE COMPLAINT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Limb Pain

  MAUDE report 16940773 ↗
• InjurySep 21, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  (B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A BED. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. WE WILL FILE A FOLLOW UP IF ADDITIONAL DATA BECOMES AVAILABLE. THE DEVICE WAS INSTALLED WITHOUT THE HEADBOARD AND FOOTBOARD. THE MATTRESS SLIPPED OFF THE BED. THE END USER THREW HERSELF TO THE FLOOR BECAUSE SHE WAS MISERABLE. SHE WAS TAKEN TO THE HOSPITAL WHERE SHE STAYED OVERNIGHT. SHE BROKE HER ARM IN THE FALL. THE DEVICE DID NOT PRECIPITATE THE INCIDENT.

  Patient problems: Fall; Limb Fracture

  MAUDE report 12510847 ↗