BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 2080282 · Received March 31, 2011

    Report

    Report Number
    2027969-2011-00657
    Event Type
    Malfunction
    Date Received
    March 31, 2011
    Date of Event
    March 9, 2011
    Report Date
    March 31, 2011
    Manufacturer
    ALERE SAN DIEGO, INC.
    Product Code
    GJS
    PMA / PMN Number
    K021923
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, 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 THE LAB. RESULTS AS FOLLOWS:" DATE: (B)(6) 2011; INRATIO: 1.1, 3.6, 2.7; LAB: 3.1. THERAPEUTIC RANGE= 2-3. PATIENT HAD NORMAL HEMATOCRIT; HAS HISTORY OF ANEMIA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC. 100139 239278

    Patients

    Seq Age Sex Outcome Treatment
    1