BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DTT DIGITAL THERMOMETER

    MDR report key: 7259305 · Received February 8, 2018

    Report

    Report Number
    MW5075138
    Event Type
    Injury
    Date Received
    February 8, 2018
    Date of Event
    December 5, 2017
    Report Date
    February 7, 2018
    Manufacturer
    K-JUMP HEALTH CO., LTD.
    Product Code
    FLL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I USED THIS THERMOMETER BUT NEVER GAVE ACCURATE READING, SO I USED ANOTHER THERMOMETER ALL THE TIME TO MAKE SURE. IT NEVER POINTS OUT FEVER. NOTHING SERIOUS HAPPENS AS I CHECKED ON ANOTHER THERMOMETER BUT IF I DON'T HAVE ANOTHER THERMOMETER THEN SOMETHING COULD HAPPEN TO MY BABY AND MY OTHER KIDS. NOW I WANT TO COMPLAIN AND CALL (B)(4) SO NO ONE ANSWERING AND EVEN NO EMAIL IS GOING TO THEM. I SPENT $(B)(6), BUT IT'S NOT WORTH IT. "IS THERE ANY WAY THAT I CAN GET A REPLACEMENT OR MY MONEY BACK", I BOUGHT IN USA BUT NOW IN (B)(6). PLEASE LET ME KNOW. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    101221 DTT DIGITAL THERMOMETER THERMOMETER FLL K-JUMP HEALTH CO., LTD. KD 2201

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention