Drive 15571HRRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00822383963600), received between Jan 22, 2025 and Jun 30, 2026 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 30, 2026Material Integrity Problem

  DRIVE MEDICAL WAS NOTIFIED OF AN INCIDENT INVOLVING AN ADJUSTABLE BED BY THE END USER'S WIFE WHO REPORTED THAT THE BED RAIL BROKE RESULTING IN THE END USER FALLING ONTO THE BED RAIL AND HITTING HIS HEAD.THE FOLLOWING DAY THE END USER WAS NOT "ACTING RIGHT" AND EMERGENCY MEDICAL SERVICES WERE CONTACTED. AND THE END USER WAS TAKEN TO THE HOSPITAL AND ADMITTED.ATTEMPTS TO GATHER ADDITIONAL INFORMATION HAVE BEEN UNSUCCESSFUL.AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS,DRIVE MEDICAL WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

  Patient problems: Insufficient Information

  MAUDE report 25664948 ↗
• InjuryJun 5, 2026Break

  DRIVE MEDICAL WAS NOTIFIED OF AN INCIDENT INVOLVING AN ADJUSTABLE BED BY THE END USER'S WIFE WHO REPORTED THAT THE BED RAIL BROKE RESULTING IN THE END USER FALLING ONTO THE BED RAIL AND HITTING HIS HEAD. THE FOLLOWING DAY THE END USER WAS NOT "ACTING RIGHT" AND EMERGENCY MEDICAL SERVICES WERE CONTACTED, AND THE END USER WAS TAKEN TO THE HOSPITAL AND ADMITTED. ATTEMPTS TO GATHER ADDITIONAL INFORMATION HAVE BEEN UNSUCCESSFUL. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE MEDICAL WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

  Patient problems: Insufficient Information

  MAUDE report 25410504 ↗
• InjuryJan 22, 2025Thermal Decomposition of Device; Thermal Decomposition of Device

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BED BY A LETTER FROM AN ATTORNEY, STATING THAT THE END USER WAS IN BED WHEN THE MOTOR OF THE BED AND MATTRESS ALLEGEDLY CAUGHT ON FIRE, CAUSING SECOND AND THIRD DEGREE BURNS TO THEIR LEGS. THERE WAS NO FURTHER INFORMATION PROVIDED. DRIVE WILL COOPERATE AND PARTICIPATE IN THE LITIGATION PROCESS TO GATHER FURTHER INFORMATION AS TO THE ORIGIN AND CAUSE OF THE FIRE. 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: Full thickness (Third Degree) Burn; Partial thickness (Second Degree) Burn

  MAUDE report 21208827 ↗