BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    MDR report key: 1061548 · Received June 17, 2008

    Report

    Report Number
    1823260-2008-04793
    Event Type
    Malfunction
    Date Received
    June 17, 2008
    Date of Event
    June 12, 2008
    Report Date
    June 17, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K010362
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    RN REPORTED ADVANTAGE METER RESULT OF HI MG/DL, WHICH ON THE ADVANTAGE SYSTEM INDICATES A VALUE IN EXCESS OF 600 MG/DL, AND A PROFESSIONAL METER RESULT OF 212 MG/DL WITHIN 10 MINUTES ON THE ADVANTAGE SYSTEM. CUSTOMER REPORTED NO SYMPTOMS, DID NOT TREAT OR ACT ON RESULTS. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE SYSTEM, REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK COMFORT CURVE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS - LFR LFR ROCHE DIAGNOSTICS 550071

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR LANTUS: 60 UNITS/DAY 11 YEARS| METFORMIN: 1000MG/DAY 13 YEARS