BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DIGITAL THERMOMETER

    MDR report key: 6883211 · Received September 20, 2017

    Report

    Report Number
    MW5072253
    Event Type
    Injury
    Date Received
    September 20, 2017
    Date of Event
    September 29, 2016
    Report Date
    September 19, 2017
    Manufacturer
    BESTMED, LLC / K-JUMP HEALTH CO., LTD.
    Product Code
    FLL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Narratives

    Description of Event or Problem · 1

    MY CHILD HAD BEEN COME DOWN WITH A FEVER SO I WENT INTO A (B)(6), I BOUGHT THE DIGITAL THERMOMETER. I READ HER TEMP AT 102 SO I GAVE HER MEDICINE TO REDUCE THE FEVER. I TOOK IT AGAIN WHEN SHE WARMED UP AND IT WAS SLIGHTLY LOWER. I DIDN'T TAKE HER IN TO THE HOSPITAL IMMEDIATELY. AFTER SHE BEGAN TO HAVE FAST BREATHING AND A POUNDING CHEST DID I TAKE HER IN. SHE WAS ACTUALLY 3 DEGREES HIGHER THAN WHAT THE THERMOMETER INDICATED. MY CHILD WAS AT A 104 WHEN WE HIT THE ER. SHE HAD BEEN POSSIBLY AT A 105 WHILE I'M THINKING THE THERMOMETER WAS CORRECT. SHE HAD PNEUMONIA AND WAS TREATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    658605 DIGITAL THERMOMETER THERMOMETER, ELECTRONIC FLL BESTMED, LLC / K-JUMP HEALTH CO., LTD. KI-8190 1410

    Patients

    Seq Age Sex Outcome Treatment
    1 14 MO Life Threatening