DRIVEMEDICAL STD22DDA-ELRRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383191898), received between Jul 11, 2022 and Jul 11, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Fold, Unfold or 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.

• InjuryJul 11, 2022Difficult to Fold, Unfold or Collapse; Difficult to Fold, Unfold or Collapse

  DRIVE DEVILBISS HEALTHCARE RECEIVED A COMPLAINT INVOLVING A WHEELCHAIR FROM AN ATTENDANT TO AN END USER, WHO REPORTED THAT THE END USER "SLID OUT OF CHAIR AND CUT HER LEG ON EITHER THE FOOTREST OR FORK ASSEMBLY. THE ATTENDANT ALSO NOTED THAT "IT IS UNCLEAR WHAT CAUSED THE PATIENT TO SLIP OUT OF THE CHAIR." THE CUT WAS REPORTEDLY TREATED IN THE EMERGENCY ROOM, BUT BECAME INFECTED AND HAD TO BE TREATED FURTHER. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT TO EVALUATE IT.

  Patient problems: Laceration(s)

  MAUDE report 14982330 ↗