BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    MDR report key: 1780595 · Received September 26, 2007

    Report

    Report Number
    1823260-2007-08408
    Event Type
    Malfunction
    Date Received
    September 26, 2007
    Date of Event
    August 31, 2007
    Report Date
    September 26, 2007
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K010362
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    LAY USER/PATIENT

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY OBTAINED RESULTS OF 17 MG/DL AND 167 MG/DL ON THE ADVANTAGE SYSTEM WITHIN 10 MINUTES. NO ACTION TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT SYSTEM, HOWEVER, STRIPS ARE UNAVAILABLE FOR RETURN.

    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 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR COREG - 2 YRS - 3.125 MG/DAY| GLUCOTROL - YEARS 5 MG/DAY| LASIX - 3 YRS - 20MG/DAY| LISINOPRIL - 3 YRS - 10MG/DAY| PREDNIZONE - YEARS - 6 MG/DAY| LESCOL - YEARS - 20MG/DAY| COUMADIN - 3 YRS - 5MG/DAY| METHOTREXATE - 4-5 YEARS - 10 MG/WEEK| NORVASC - YEARS - 5 MG/DAY| LANOXIN - YEARS - 0.25 MG/DAY| FOSAMAX - 3 YRS - 35MG/WEEK