BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRECISION XTRA/OPTIUM

    MDR report key: 1012144 · Received May 16, 2007

    Report

    Report Number
    2954323-2007-07962
    Event Type
    Malfunction
    Date Received
    May 16, 2007
    Date of Event
    April 16, 2007
    Report Date
    May 16, 2007
    Manufacturer
    ABBOTT DIABETES CARE INC., UK
    Product Code
    NBW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    NO INFORMATION

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRECISION XTRA/OPTIUM BLOOD GLUCOSE METER NBW ABBOTT DIABETES CARE INC., UK NA 41661

    Patients

    Seq Age Sex Outcome Treatment
    1 NI