BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONAIR CORPORATION

    MDR report key: 10388145 · Received August 10, 2020

    Report

    Report Number
    1222304-2020-00008
    Event Type
    Malfunction
    Date Received
    August 10, 2020
    Date of Event
    July 3, 2020
    Report Date
    July 6, 2020
    Manufacturer
    CONAIR CORPORATION
    Product Code
    MNW
    UDI-DI
    00074108337290
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    07/16/2020:THE CONSUMER ACCEPTED A PRODUCT REPLACEMENT. THEREFORE, THE CONSUMER WILL NOT BE RETURNED THE PRODUCT TO THE MANUFACTURER FOR AN INVESTIGATION.

    Description of Event or Problem · 1

    7/6/2020: THE CONSUMER CLAIMS THE PRODUCT EXPLODED. THE CONSUMER ACCEPTED A REPLACEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    853358 CONAIR CORPORATION BMI SCALE MNW CONAIR CORPORATION WW711XF 00074108337290

    Patients

    Seq Age Sex Outcome Treatment
    1 Other