Drive 18302GDELRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383143170), received between Oct 26, 2023 and Oct 26, 2023 — classified as 1 death.

The most frequently reported specific device problem is “Fire” (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.

• DeathOct 26, 2023Fire; Fire

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING AN OXYGEN REGULATOR INVOLVED IN AN IGNITION EVENT BY A LETTER FROM AN ATTORNEY, WHICH ALLEGES THAT THE RESULTING FIRE WAS CAUSED BY AN ALLEGED DEFECT IN THE REGULATOR. THE FIRE RESULTED IN PROPERTY DAMAGE. ALTHOUGH A DEATH WAS REPORTED, THE MEDICAL EXAMINER DID NOT ATTRIBUTE THE DEATH TO THE DEVICE. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Cardiac Arrest

  MAUDE report 18016213 ↗