BEUDAMED
    FDA Adverse Event Summary report: N

    LIFEFACTORY SILICONE TEETHING RING

    MDR report key: 8922696 · Received August 21, 2019

    Report

    Report Number
    MW5089242
    Date Received
    August 21, 2019
    Date of Event
    July 1, 2019
    Report Date
    July 28, 2019
    Manufacturer
    UNK
    Product Code
    KKO
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Narratives

    Description of Event or Problem · 1

    MY SON HAD BEEN USING THIS TEETHING RING. WHEN HE TWISTED IT AROUND, I COULD SEE CRACKS IN IT. UPON INSPECTING IT, I FOUND ONE SMALL PIECE OF IT IS MISSING AND THERE ARE CRACKS ALL AROUND IT. LIGHT GREEN, MANUFACTURED DATE: 11/2013. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    712643 LIFEFACTORY SILICONE TEETHING RING RING, TEETHING, FLUID-FILLED KKO UNK

    Patients

    Seq Age Sex Outcome Treatment
    1