BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 2134942 · Received May 16, 2011

    Report

    Report Number
    2027969-2011-01080
    Event Type
    Malfunction
    Date Received
    May 16, 2011
    Date of Event
    April 25, 2011
    Report Date
    May 16, 2011
    Manufacturer
    ALERE SAN DIEGO, INC.
    Product Code
    GJS
    PMA / PMN Number
    K021923
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, 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: DATE: 04/25/2011; INRATIO: 4.5; DOCTOR'S POC: 3.1. (22 MINS BETWEEN TESTS). CALLER WASN¿T EXACTLY SURE WHAT THE DOCTOR'S METER READING WAS OR THE TYPE OF METER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC. 100071 236690

    Patients

    Seq Age Sex Outcome Treatment
    1