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DeVilbiss 6910D-DRRecalls & reported problems

Devilbiss Healthcare LLC · Portable Compressor · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885304002529), received between Sep 28, 2021 and Sep 28, 2021 — classified as 1 malfunction.

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

Most reported problems

Device problems

  • Fire1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionSep 28, 2021Fire; Fire

    DEVILBISS HEALTHCARE IS THE MANUFACTURER OF THE DEVICE WHICH IS A NEBULIZER. WE ARE AWAITING RETURN OF THE DEVICE FOR EVALUATION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN ADDITIONAL DATA IS AVAILABLE. WE ARE FILING THIS REPORT IN AN OVER ABUNDANCE OF CAUTION. THE DEVICE WAS ACQUIRED ONE YEAR AGO. THE USER NEVER NOTICED IT OVERHEATING OR A BURNING SMELL BEFORE. HOWEVER, WITHIN THE LAST WEEK HE NOTICED THE NOISE LEVEL OF THE DEVICE INCREASED. THE DEVICE STARTED SMOKING AND CAUGHT ON FIRE DURING THE USER'S REGULAR MORNING TREATMENT. HE CHANGED THE FILTERS AND UPDATED THE HOSES AS NECESSARY. NO INJURIES OCCURRED NOR DID ANY PROPERTY DAMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12543633 ↗

Other Compressor, Air, Portable devices

All Compressor, Air, Portable devices →

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