Drive SFPRO417FS-21Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383991788), received between Jul 21, 2021 and Jul 21, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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 21, 2021Break; Break

  (B)(6) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A POWER MOBILITY SCOOTER. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. IN AN OVERABUNDANCE OF CAUTION WE ARE FILING THIS REPORT. WE WILL SUBMIT A FOLLOWUP REPORT IF ANY ADDITIONAL DATA BECOMES AVAILABLE. WHILE THE CUSTOMER WAS CROSSING THE STREET WITHOUT USING A CURB WHEN BOTH WHEELS AND AXEL CAME OFF DEVICE FROM THE REAR APPARATUS. SHE FELL IN THE STREET,HIT HER HEAD,AND WENT TO THE HOSPITAL. SHE DID NOT HAVE ANY SERIOUS INJURIES, ONLY A STIFF NECK. SHE USES THE DEVICE AS AN ALTERNATIVE TO TAKING AN UBER OR BUS.

  Patient problems: Bruise/Contusion; Fall

  MAUDE report 12201881 ↗