BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK AVIVA TEST STRIPS

    MDR report key: 1052280 · Received May 23, 2008

    Report

    Report Number
    1823260-2008-04274
    Event Type
    Malfunction
    Date Received
    May 23, 2008
    Date of Event
    May 20, 2008
    Report Date
    May 23, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K043474
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    LAY USER/PATIENT

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY RECEIVED RESULTS OF 232 MG/DL AND 65 MG/DL WITHIN 10 MINUTES ON THE AVIVA SYSTEM. LOW BLOOD GLUCOSE SYMPTOMS REPORTED WITH THESE RESULTS; CUSTOMER WAS ABLE TO SELF TREAT. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT SYSTEM AND REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK AVIVA TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS - LFR LFR ROCHE DIAGNOSTICS 300881

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK UNK INSULIN