BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ACTIVE TEST STRIPS

    MDR report key: 1241639 · Received November 19, 2008

    Report

    Report Number
    1823260-2008-08585
    Event Type
    Malfunction
    Date Received
    November 19, 2008
    Date of Event
    October 25, 2008
    Report Date
    November 19, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K021827
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    LAY USER/PATIENT

    Narratives

    Description of Event or Problem · 1

    REPORTER ALLEGED OBTAINING A DISCREPANT BLOOD GLUCOSE RESULT OF 189 MG/DL BACK TO BACK WITH A RESULT OF 97 MG/DL ON THE ACTIVE S SYSTEM WHEN TESTING WAS PERFORMED WITHIN 10 MINUTES. NO ACTIONS WERE REPORTED TAKEN OR TREATMENT RECEIVED. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE SUSPECT DEVICE AND REPLACEMENT PRODUCT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK ACTIVE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS - LFR LFR ROCHE DIAGNOSTICS 22974232

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR METFORMIN - 500MG 4 TIMES DAILY| PRAVACHOL - 40MG DAILY| NORVASC - SINCE 1990S 5MG DAILY| ZIAC - 2.5MG DAILY| ZETIA - 10MG NIGHTLY