DRIVEMEDICAL BLS18FBD-ELRRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383241142), received between Oct 20, 2021 and Oct 20, 2021 — 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 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 20, 2021Fracture; Fracture

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. A FOLLOW-UP SUBMISSION WILL BE FILED WHEN ADDITIONAL INFORMATION IS AVAILABLE. WHILE IN USE TRAVELING UP A HILL THE SIDE FRAME OF THE DEVICE BROKE. THE OCCUPANT HE FELL OUT OF THE CHAIR AND ROLLED DOWN THE SIDEWALK, SCRAPPING HIS ARMS, LEGS, AND HANDS AND BRUISING HIS HIP. THEY TOOK HIM TO THE EMERGENCY ROOM RIGHT AFTER THE INCIDENT. HE HAD BEEN ATTENDING THERAPY TO RELEARN TO WALK. THIS INCIDENT SET HIM BACK FROM MOVING FORWARD WITH LEARNING TO WALK.

  Patient problems: Easy Bruising; Fall

  MAUDE report 12667005 ↗