BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONAIR

    MDR report key: 14604028 · Received June 6, 2022

    Report

    Report Number
    1222304-2022-00021
    Event Type
    Malfunction
    Date Received
    June 6, 2022
    Date of Event
    May 20, 2022
    Report Date
    June 6, 2022
    Manufacturer
    CONAIR LLC
    Product Code
    MNW
    UDI-DI
    74108376930
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    ON (B)(6) 2022 - THE CONSUMER DISCARDED THE PRODUCT AND DID NOT ACCEPT A REPLACEMENT. THE CONSUMER CONTACTED OUR CUSTOMER SERVICE DEPARTMENT TO MAKE US AWARE.

    Description of Event or Problem · 0

    ON (B)(6) 2022 - THE CONSUMER CLAIMS THE PRODUCT SHATTERED. INJURIES DID NOT OCCUR. THE CONSUMER DISCARDED THE PRODUCT. THE CONSUMER DID NOT REQUEST A REPLACEMENT AND ONLY WANTED TO INFORM OUR CS TEAM OF THE INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    889522 CONAIR BMI SCALE MNW CONAIR LLC WW706XF 74108376930

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Other