BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COAGUCHEK S SYSTEM

    MDR report key: 1761163 · Received July 13, 2007

    Report

    Report Number
    1823260-2007-06077
    Event Type
    Malfunction
    Date Received
    July 13, 2007
    Date of Event
    June 28, 2007
    Report Date
    July 13, 2007
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    JPA
    PMA / PMN Number
    K962571
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    LAY USER/PATIENT

    Narratives

    Description of Event or Problem · 1

    CALLER STATES THE PATIENT TESTED 2.1 INR ON THE COAGUCHEK SYSTEM AND 3.3 INR ON A COMPARISON LAB. NO ACTION TAKEN ON DEVICE RESULT. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT SYSTEM AND REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COAGUCHEK S SYSTEM PROTHROMBIN TIME TEST STRIPS - JPA JPA ROCHE DIAGNOSTICS 566A-15

    Patients

    Seq Age Sex Outcome Treatment
    1 NA OMEGA3| CELEBREX - 200MG/DAY| ASPIRIN - 81MG/DAY| NEXIUM - 40MG/DAY| COUMADIN - ALT 4.5MG/5MG| VITAMIN