BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 2123366 · Received June 10, 2011

    Report

    Report Number
    2027969-2011-01302
    Event Type
    Malfunction
    Date Received
    June 10, 2011
    Date of Event
    May 11, 2011
    Report Date
    June 10, 2011
    Manufacturer
    ALERE SAN DIEGO, INC
    Product Code
    GJS
    PMA / PMN Number
    K021923
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION PENDING.

    Description of Event or Problem · 1

    CUSTOMER ALLEGES DISCREPANT RESULTS WITH METER COMPARED TO ANOTHER POINT OF CARE (POC) METER: DATE: (B)(6) 2011; INRATIO: 4.7. DATE: (B)(6) 2011; INRATIO: 3.7; POC METER: 2.8. PT'S TARGET THERAPEUTIC RANGE IS 2.5-3.5. PT SKIPPED HER DOSE ON (B)(6) 2011 AFTER GETTING A 4.7 RESULT ON HER METER.

    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