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Drive SF1320-CFRecalls & reported problems

Drive Devilbiss Healthcare · Spitfire 1320, 12AH, Carbon Fiber Shroud · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383984025), received between Aug 6, 2018 and Aug 6, 2018 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Fall1
  • Hip Fracture1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 6, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A 3 WHEELED POWER SCOOTER. THE UNIT WAS RETURNED TO THE SELLING AGENT AND IS UNAVAILABLE FOR INVESTIGATION. THE CUSTOMER STATES THAT HER HUSBAND WAS ON THE ITEM GOING SLOWLY THE DAY HE RECEIVED IT. HE WAS TURNING IN THE DRIVEWAY WHEN THE ITEM TILTED. HE PUT HIS FOOT DOWN TO CATCH THE FALL. HE WAS TAKEN TO THE HOSPITAL WHERE THEY TOOK X-RAYS WHICH REPORTEDLY SHOWED A MINIMAL FRACTURE IN HIS HIP. AT THE TIME OF THIS REPORT THE END-USER WAS IN REHAB WITH NO PROSPECT OF SURGERY. HE ALSO IS REPORTED TO HAVE SUFFERED "BRUSH BURNS" ON HIS ARM AND SOME SCABS ON HIS HAND FROM STOPPING THE UNIT FROM TIPPING.

    Patient problems: Fall; Hip Fracture

    MAUDE report 7751786 ↗

Other VEHICLE, MOTORIZED 3-WHEELED devices

All VEHICLE, MOTORIZED 3-WHEELED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.