DRIVEMEDICAL DFL19-BLRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383137377), received between Jul 26, 2023 and Jul 26, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device 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.

• InjuryJul 26, 2023Use of Device Problem; Use of Device Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A TRANSPORT CHAIR BY AN END USER, WHO STATED THAT AS SHE ATTEMPTED TO SIT IN THE CHAIR, SHE "WAS HOLDING ONTO THE ARM RESTS [AND]... WHEN SHE SAT DOWN THE CHAIR TIPPED OVER BACKWARDS AND HIT THE BACK OF HER HEAD ON THE PAVEMENT." THE END USER REPORTED THAT SHE SUSTAINED A CONCUSSION AND SOUGHT MEDICAL TREATMENT, INCLUDING MEDICATION FOR HEADACHES AND NAUSEA. THE END USER CONFIRMED THAT THERE WAS NO DEFECT DETECTED WITH HER UNIT. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Concussion; Fall; Head Injury

  MAUDE report 17399024 ↗