BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK COMPACT TEST DRUM

    MDR report key: 1172566 · Received September 19, 2008

    Report

    Report Number
    1823260-2008-07014
    Event Type
    Malfunction
    Date Received
    September 19, 2008
    Date of Event
    September 10, 2008
    Report Date
    September 19, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    LAY USER/PATIENT

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTED BLOOD GLUCOSE RESULTS OF 117 MG/DL, 110 MG/DL, AND 231 MG/DL WITHIN 10 MINUTES ON THE COMPACT PLUS SYSTEM; ALSO REPORTED BLOOD GLUCOSE RESULTS OF 95 MG/DL, 97 MG/DL, 102 MG/DL, 295 MG/DL, AND 122 MG/DL WITHIN 10 MINUTES ON THE COMPACT PLUS SYSTEM. CUSTOMER REPORTED NO SYMPTOMS, DID NOT TREAT OR ACT ON RESULTS. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE SYSTEM, REPLACEMENT WAS SENT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR "BLADDER MEDICATION" 15-25MG - 3-4 MONTHS| "HEART BURN PILLS"| VALIUM - 3-4 MONTHS| METHADONE 30 MG/DAY - 1 YEAR