BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIONAIRE

    MDR report key: 3961113 · Received May 27, 2014

    Report

    Report Number
    3008559271-2014-00095
    Event Type
    Malfunction
    Date Received
    May 27, 2014
    Report Date
    May 27, 2014
    Manufacturer
    SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTIONS
    Product Code
    KFZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CONSUMER CLAIMS HIS HUMIDIFIER MELTED ON THE BOTTOM AND DAMAGED HIS CARPET. THERE WERE NO REPORTS OF INJURY WITH THIS INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    311950 BIONAIRE HUMIDIFIER KFZ SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTIONS BUL8000 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1