BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO 2

    MDR report key: 2002630 · Received February 8, 2011

    Report

    Report Number
    2027969-2011-00274
    Event Type
    Malfunction
    Date Received
    February 8, 2011
    Date of Event
    January 18, 2011
    Report Date
    February 8, 2011
    Manufacturer
    ALERE SAN DIEGO, INC.
    Product Code
    GJS
    PMA / PMN Number
    K072727
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION PENDING.

    Description of Event or Problem · 1

    CALLER ALLEGED DISCREPANT RESULTS USING THE INRATIO METER: RESULTS AS FOLLOWS: DATE: (B)(6) 2011; INRATIO: 5.2; LAB: 11.0. INRATIO TEST AND LAB DRAW WERE DONE AT THE SAME TIME. DISCREPANT RESULT OCCURRED AFTER METER WAS DROPPED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO 2 PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC. 100139 234880

    Patients

    Seq Age Sex Outcome Treatment
    1