BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    MDR report key: 1760968 · Received July 17, 2007

    Report

    Report Number
    1823260-2007-06171
    Event Type
    Malfunction
    Date Received
    July 17, 2007
    Date of Event
    July 5, 2007
    Report Date
    July 17, 2007
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K010362
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DE, US
    Reporter Occupation
    LAY USER/PATIENT

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY RECEIVED RESULTS OF 401 MG/DL AND 172 MG/DL WITHIN 10 MINUTES ON THE ADVANTAGE SYSTEM. NO ACTIONS TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT DEVICE AND REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK COMFORT CURVE TEST STRIPS BLOOD GLUCOSE MONITORING DEVICE - LFR LFR ROCHE DIAGNOSTICS 549532

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR GLYBURIDE - 5MG TWICE DAILY -1 YEAR| FUROSEMIDE - 40MG ONCE DAILY - 5 YEARS| ATENOLOL - 50MG ONCE DAILY - 5 YEARS OR MORE| FEKIDUOID - 5MG ONCE DAILY - 5 YEARS OR MORE| LISINOPRIL - 40MG ONCE DAILY - 5 YEARS OR MORE| ZOCOR - 20MG ONCE DAILY - 5 YEARS OR MORE