DRIVEMEDICAL STD22ECDDA-SFRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383136011), received between Dec 5, 2022 and Dec 5, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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 5, 2022Fracture; Fracture

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR CHAIR BY AN END USER'S SON, WHO STATED THAT THE END USER "PASSED OUT" OUT WHILE IN THE CHAIR AND THE FRAME OF THE CHAIR BROKE AND CAUSED THE END USER TO FALL TO THE FLOOR, SUSTAINING A FRACTURE TO HIS BACK. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Fall; Spinal Column Injury

  MAUDE report 15915083 ↗