BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FREESTYLE FREEDOM

    MDR report key: 1070205 · Received July 3, 2008

    Report

    Report Number
    2954323-2008-02199
    Event Type
    Malfunction
    Date Received
    July 3, 2008
    Date of Event
    June 6, 2008
    Report Date
    July 3, 2008
    Manufacturer
    ABBOTT DIABETES CARE INC, USA
    Product Code
    LFR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER DID NOT PROVIDE METER SERIAL NUMBER, STRIP LOT NUMBER AND CONTROL SOLUTION. IN ADDITION, THE CUSTOMER'S PRODUCT HAS BEEN REQUESTED BACK FOR INVESTIGATION, HOWEVER, CUSTOMER REFUSED TO RETURN METER. NOTE: IT SHOULD BE NOTED THAT THIS METER DOES NOT GIVE A VALUE FOR READING GREATER THAN 500 MG/DL. A "HI" DISPLAY MESSAGE INDICATES A READING GREATER THAN 500 MG/DL.

    Description of Event or Problem · 1

    CUSTOMER REPORTED RECEIVING ERRATIC READINGS ON THEIR FREESTYLE FREEDOM BLOOD GLUCOSE MONITOR WITHIN 10 MINUTES. RESULTS OF 87 MG/DL AND 501 MG/DL WERE PLOTTED ON A PARKES ERROR GRID. THE RESULTS FELL INTO THE "C" ZONES SHOWING THE DIFFERENCE IN VALUES TO BE CLINICALLY SIGNIFICANT. THERE WAS NO REPORT OF DEATH, SERIOUS INJURY OR MISTREATMENT ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FREESTYLE FREEDOM BLOOD GLUCOSE MONITORING SYSTEM LFR ABBOTT DIABETES CARE INC, USA NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA