BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COAGUCHEK XS SYSTEM

    MDR report key: 1770988 · Received November 13, 2007

    Report

    Report Number
    1823260-2007-09864
    Event Type
    Malfunction
    Date Received
    November 13, 2007
    Date of Event
    October 26, 2007
    Report Date
    November 13, 2007
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    GJS
    PMA / PMN Number
    K062925
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO PATIENT INFORMATION PROVIDED.

    Description of Event or Problem · 1

    CALLER REPORTS PATIENT TESTED 1.2 INR ON THE COAGUCHEK XS AND 2.19 INR ON A COMPARISON LABORATORY. NO ADVERSE EVENT REPORTED. NO TREATMENT GIVEN BASED ON THE DEVICE RESULT. REQUESTED RETURN OF SUSPECT SYSTEM AND REPLACEMENT SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COAGUCHEK XS SYSTEM PROTHROMBIN TIME TEST STRIPS - GJS GJS ROCHE DIAGNOSTICS 20154731

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK