BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRECISION QID BLOOD GLUCOSE MONITOR

    MDR report key: 283658 · Received June 27, 2000

    Report

    Report Number
    MW1019182
    Event Type
    Injury
    Date Received
    June 27, 2000
    Date of Event
    May 25, 2000
    Report Date
    May 26, 2000
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    CFR
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    MACHINE (PRECISION QID) NOT WORKING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRECISION QID BLOOD GLUCOSE MONITOR BLOOD GLUCOSE MONITOR CFR ABBOTT LABORATORIES, INC. Q4525-0104 83281

    Patients

    Seq Age Sex Outcome Treatment
    1 * Disability