BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 810224 · Received January 12, 2007

    Report

    Report Number
    2954730-2007-00022
    Event Type
    Malfunction
    Date Received
    January 12, 2007
    Date of Event
    January 4, 2007
    Report Date
    January 10, 2007
    Manufacturer
    HEMOSENSE, INC.
    Product Code
    JPA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    INRATIO PRECISION DATA PROVIDED BY END-USER LOT 060541: FIRST TEST INR = 7.2, SECOND TEST INR = 2.6, THIRD TEST INR = 1.1, MEAN = 3.6, SD = 3.17, %CV = 87%. THE %CV IS GREATER THAN 20%. PER INTERNAL PROCEDURE, THE PRECISION FAIL THE CRITERIA FOR PRECISION. PRODUCTS WILL BE TESTED.

    Description of Event or Problem · 1

    CALLED ALLEGED IMPRECISION WITH INRATIO. RESULTS AS FOLLOWS: FIRST TEST INR = 7.2, SECOND TEST INR = 2.6, THIRD TEST INR = 1.1.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST JPA HEMOSENSE, INC. * 060541

    Patients

    Seq Age Sex Outcome Treatment
    1 *