BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COAGUCHEK S SYSTEM

    MDR report key: 1771214 · Received February 15, 2008

    Report

    Report Number
    1823260-2008-01610
    Event Type
    Malfunction
    Date Received
    February 15, 2008
    Date of Event
    January 31, 2008
    Report Date
    February 15, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    JPA
    PMA / PMN Number
    K974569
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CALLER STATES THE PATIENT TESTED 2.5 INR ON THE COAGUCHEK S SYSTEM AND 1.7 INR ON A COMPARISON LAB. CALLER WAS UNSURE OF ACTION TAKEN, HOWEVER STATES SHE THINKS ACTION WAS 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 565A-B3

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK