DRIVEMEDICAL SSP218DDA-SFRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383140469), received between Oct 11, 2018 and Oct 11, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Material Integrity 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 18, 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.

• InjuryOct 11, 2018Material Integrity Problem; Material Integrity Problem

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. END-USER WILL NOT PROVIDE PMS TEAM WITH DEVICE UNTIL SETTLEMENT IS REACHED. THE SERIAL NUMBER HE PROVIDED IS NOT IN OUR SYSTEM. IN AN OVERABUNDANCE OF CAUTION WE ARE FILING THIS MEDWATCH REPORT. END-USER WAS SITTING AT THE TABLE EATING WHEN THE SEAT REPORTEDLY DROPPED THROUGH THE FRAME. HE ADVISED THAT SOME OF THE UPHOLSTERY SCREWS WERE NOT PROPERLY THREADED THROUGH THE FRAME. HE FELL AND SUFFERED CONTUSIONS AND LACERATIONS. HE VISITED THE DOCTOR AND WAS DIAGNOSED WITH A FRACTURE OF THE 11TH VERTEBRAE.

  Patient problems: Bone Fracture(s); Contusion; Laceration(s)

  MAUDE report 7958413 ↗