BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO2

    MDR report key: 3060902 · Received April 10, 2013

    Report

    Report Number
    2027969-2013-00289
    Event Type
    Malfunction
    Date Received
    April 10, 2013
    Date of Event
    April 5, 2013
    Report Date
    April 10, 2013
    Manufacturer
    ALERE SAN DIEGO, INC.
    Product Code
    GJS
    PMA / PMN Number
    K092987
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION PENDING.

    Description of Event or Problem · 1

    "CALLER ALLEGED DISCREPANT RESULTS COMPARED WITH LAB. RESULTS ARE AS FOLLOWS:" DATE: (B)(6) 2013; INRATIO2: 1.0; LAB: 2.0. TIME BETWEEN TESTS: 30 MINUTES. THERAPEUTIC RANGE: NOT PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    148244 INRATIO2 PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC. 100139 281267

    Patients

    Seq Age Sex Outcome Treatment
    1