BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 1970391 · Received January 25, 2011

    Report

    Report Number
    1823260-2011-00383
    Event Type
    Malfunction
    Date Received
    January 25, 2011
    Date of Event
    January 4, 2011
    Report Date
    February 18, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CALLER REPORTED COMPACT PLUS SYSTEM BLOOD GLUCOSE RESULTS OF 281 MG/DL AND 103 MG/DL WITHIN 10 MINUTES. REPORTED NO ADVERSE EVENT RELATIVE TO DISCREPANCY. A REQUEST WAS MADE FOR THE RETURN OF THE CONTROLS, METER AND STRIPS, REPLACEMENT SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 207257

    Patients

    Seq Age Sex Outcome Treatment
    1 062 YR SIMVASTATIN| LANTUS| METFORMIN| AMLODIPINE BESYLATE| FUROSEMIDE| ASPIRIN| DIOVAN| NOVOLOG