BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK AVIVA TEST STRIPS

    MDR report key: 1083620 · Received July 29, 2008

    Report

    Report Number
    1823260-2008-05838
    Event Type
    Malfunction
    Date Received
    July 29, 2008
    Date of Event
    July 25, 2008
    Report Date
    July 29, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K043474
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    LAY USER/PATIENT

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTEDLY OBTAINED A 271MG/DL AND 114MG/DL ON THE ACCU-CHEK AVIVA SYSTEM WITHIN A TEN MINUTE TIMEFRAME. NO REPORTED ACTIONS TAKEN OR TREATMENT RENDERED. NO ADVERSE EVENT REPORTED. THE CUSTOMER STATES THAT SHE HAD HER HAND ON A SYRUP BOTTLE AND DID NOT WASH HER HANDS PRIOR TO OBTAINING THE 271MG/DL BLOOD GLUCOSE RESULT. NEW SYSTEM SENT TO CUSTOMER AND RETURN REQUESTED.

    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 301081

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR LEVEMIR - 1 MONTH| AVANDIA - LONG TIME| METFORMIN - "FOREVER"