BEUDAMED
    FDA Adverse Event Summary report: N

    NUBY

    MDR report key: 7663470 · Received July 3, 2018

    Report

    Report Number
    MW5078239
    Date Received
    July 3, 2018
    Date of Event
    June 1, 2018
    Report Date
    June 11, 2018
    Manufacturer
    LUV N' CARE LTD.
    Product Code
    KKO
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I BOUGHT A VIBRATING TEETHER FOR MY SON, AFTER ONLY 3 DAYS OF USING IT, IT STOPPED VIBRATING. I OPENED UP THE BACK WHERE THE BATTERY IS TO SEE IF THE BATTERY MAYBE GOTTEN MOVED, AND IT WAS FULL OF CORROSION. THIS IS VERY UNSAFE FOR A BABY TO CHEW ON. INCIDENT LOCATION: (B)(6), UNITED STATES; THIS IS MY HOME ADDRESS. RETAILER: (B)(6); RETAILER STATE: (B)(4); PURCHASE DATE: (B)(6) 2018. DOCUMENT NUMBER: (B)(4). REPORT NUMBER: (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    499664 NUBY RING, TEETHING, FLUID-FILLED KKO LUV N' CARE LTD.

    Patients

    Seq Age Sex Outcome Treatment
    1