Drive 11117N-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383226224), received between Dec 10, 2018 and Dec 10, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Collapse” (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 10, 2018Collapse; Collapse

  (B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A COMMODE. (B)(4) BECAME AWARE OF THE INCIDENT THROUGH ATTORNEY'S LETTER. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. WE WILL UPDATE THIS REPORT AS NEW INFORMATION BECOMES AVAILABLE. THE END-USER WAS HOSPITALIZED AT (B)(6) HOSPITAL WHERE SHE WAS GIVEN A BEDSIDE COMMODE TO USE. IT REPORTEDLY COLLAPSED. THE FALL AGGRAVATED PRE-EXISTING BACK ISSUES.

  Patient problems: Fall

  MAUDE report 8146148 ↗