Drive 11125KD-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383227498), received between Dec 17, 2025 and Dec 17, 2025 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 17, 2025Break; Break

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A COMMODE BY THE END USER WHO STATED THAT WHEN SHE REACHED FOR THE ARM OF THE COMMODE, THE ARM COLLAPSED CAUSING HER TO FALL. SHE SUFFERED A BRUISED ARM, WHICH WAS BANDAGED BY EMS, AND SEVERAL DISCHARGES OF HER IMPLANTED DEFIBRILLATOR, WHICH SHE REPORTED AS BEING CONNECTED TO THE FALL AND BRUISING SHE SUSTAINED. 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: Bruise/Contusion; Unspecified Heart Problem

  MAUDE report 23829806 ↗