BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 1913514 · Received November 24, 2010

    Report

    Report Number
    2027969-2010-02055
    Event Type
    Malfunction
    Date Received
    November 24, 2010
    Date of Event
    November 5, 2010
    Report Date
    November 24, 2010
    Manufacturer
    ALERE SAN DIEGO, INC
    Product Code
    GJS
    PMA / PMN Number
    K021923
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION PENDING.

    Description of Event or Problem · 1

    CUSTOMER ALLEGES DISCREPANT RESULT WITH METER COMPARED TO LAB: DATE: (B)(6) 2010, INRATIO: 4.9. DATE: (B)(6) 2010, INRATIO: 5.4. DATE: (B)(6) 2010, INRATIO: 4.8, LAB: 3.3. PT IS (B)(6) SON OF THE REPORTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC 100071 NG

    Patients

    Seq Age Sex Outcome Treatment
    1