Drive 11148-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383135052), received between Sep 18, 2025 and Sep 18, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Mechanical 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. 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjurySep 18, 2025Mechanical Problem; Mechanical Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A FOLDING COMMODE BY THE END USER'S DAUGHTER WHO STATED THAT THE DETENT BROKE WHILE IN USE CAUSING THE END USER TO FALL FORWARD AND HIT HIS HEAD ON THE BATH TUB. THE END USER IS CURRENTLY IN THE HOSPITAL WITH MULTIPLE INJURIES. ATTEMPTS HAVE BEEN MADE TO GATHER ADDITIONAL INFORMATION ON THE SPECIFIC NATURE OF THE INJURY WITH NO SUCCESS. 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: Insufficient Information

  MAUDE report 23084763 ↗