BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    MDR report key: 2070929 · Received April 27, 2011

    Report

    Report Number
    1823260-2011-02280
    Event Type
    Malfunction
    Date Received
    April 27, 2011
    Date of Event
    April 15, 2011
    Report Date
    June 15, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K010362
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY RECEIVED THE FOLLOWING RESULTS ON THE ADVANTAGE SYSTEM WITHIN 10 MINUTES WHILE USING COMFORT CURVE TEST STRIPS: 152 MG/DL, 183 MG/DL, AND 508 MG/DL. NO ACTIONS TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT DEVICE AND REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK ® COMFORT CURVE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 551479

    Patients

    Seq Age Sex Outcome Treatment
    1 078 YR AMLODIPINE| "LOSARTANPOT"| PRAVASTATIN| CARVEDILOL| JANUVIA| GLIMEPIRIDE| KNEE REPLACEMENT| STENT| PLAVIX| ASPIRIN