BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONAIR

    MDR report key: 14285861 · Received May 5, 2022

    Report

    Report Number
    1222304-2022-00011
    Event Type
    Malfunction
    Date Received
    May 5, 2022
    Date of Event
    March 28, 2022
    Report Date
    May 4, 2022
    Manufacturer
    CONAIR LLC.
    Product Code
    MNW
    UDI-DI
    74108337290
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    05042022 - THE CONSUMER ACCEPTED A REPLACEMENT PRODUCT. THEREFORE THE DEVICE WILL NOT BE RETURNED TO THE MANUFACTURER FOR AN INVESTIGATION.

    Description of Event or Problem · 0

    3/28/2022 - THE CONSUMER CLAIMS THE PRODUCT SPONTAINIOULY COMBUSTED. INJURIES DID NOT OCCUR AND THE CONSUMER ACCEPTED A REPLACEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1089092 CONAIR BMI SCALE MNW CONAIR LLC. WW711XF 74108337290

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Other