BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIONAIRE

    MDR report key: 3820053 · Received May 9, 2014

    Report

    Report Number
    3003862163-2014-00083
    Event Type
    Malfunction
    Date Received
    May 9, 2014
    Date of Event
    January 29, 2014
    Report Date
    May 8, 2014
    Manufacturer
    SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTIONS
    Product Code
    KFZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    AN ATTORNEY IS ALLEGING THAT A HUMIDIFIER CAUGHT ON FIRE AND AS A RESULT, HIS CLIENT SUFFERED FROM SMOKE INHALATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    282112 BIONAIRE HUMIDIFIER KFZ SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTIONS BWM5905 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1