Drive 12022KD-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383148250), received between Jul 19, 2022 and Jul 19, 2022 — 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.

• InjuryJul 19, 2022Mechanical Problem; Mechanical Problem

  DRIVE DEVILBISS HEALTHCARE RECEIVED A LETTER FROM AN ATTORNEY STATING THAT THE ATTORNEY'S CLIENT SUSTAINED "SERIOUS INJURY" WHILE USING A SHOWER CHAIR THAT "COLLAPSED UNDER HIM." DRIVE IS ATTEMPTING TO EVALUATE THE UNIT THROUGH THE ATTORNEY AND WILL PROVIDE AN UPDATE WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Concussion

  MAUDE report 15051209 ↗