BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SUNBEAM

    MDR report key: 3220634 · Received June 25, 2013

    Report

    Report Number
    1043899-2013-00095
    Event Type
    Malfunction
    Date Received
    June 25, 2013
    Report Date
    June 25, 2013
    Manufacturer
    SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTIONS
    Product Code
    KFZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS PRODUCT IS IN THE POSSESSION OF THE CONSUMER AND HAS NOT BEEN EXAMINED. A PREPAID LABEL HAS BEEN ISSUED TO THE CONSUMER FOR RETURN OF THE PRODUCT. CONSUMER HAS NOT RETURNED THE PRODUCT.

    Description of Event or Problem · 1

    CONSUMER ALLEGES THAT HER DAUGHTER BURNED HER HAND ON A VAPORIZER WHEN REACHING FOR A PILLOW.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    286990 SUNBEAM VAPORIZER KFZ SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTIONS 1388-800 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 Other