BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONAIR

    MDR report key: 14407558 · Received May 16, 2022

    Report

    Report Number
    1222304-2022-00018
    Event Type
    Malfunction
    Date Received
    May 16, 2022
    Date of Event
    May 10, 2022
    Report Date
    May 16, 2022
    Manufacturer
    CONAIR LLC.
    Product Code
    MNW
    UDI-DI
    74108303677
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    05/16/2022 - THE CONSUMER ACCEPTED A REPLACEMENT AND WILL NOT BE RETURNING THE DEVICE TO THE MANUFACTURER. THEREFORE AN INVESTIGATION WILL NOT OCCUR.

    Description of Event or Problem · 0

    5/16/2022 - THE CONSUMER CLAIMS THE GLASS ON THE DEVICE SHATTERED. INJURIES DID NOT OCCUR AND THE CONSUMER ACCEPTED A REPLACEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    889490 CONAIR BMI SCALE MNW CONAIR LLC. WW701XF 74108303677

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Other