BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 926024 · Received March 28, 2007

    Report

    Report Number
    2954730-2007-00136
    Event Type
    Malfunction
    Date Received
    March 28, 2007
    Date of Event
    March 6, 2007
    Report Date
    March 27, 2007
    Manufacturer
    HEMOSENSE, INC.
    Product Code
    JPA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    DISCREPANT RESULTS (ACCURACY) COMPARISON OF INRATIO TEST WITH LAB RESULTS PROVIDED BY END-USER AT TIME COMPLAINT WAS FILED: (SEE SCANNED TABLE). PER INTERNAL PROCEDURE, THE MEAN OF THE INRATIO METER AND COMPARATIVE SYSTEM INR WERE CALCULATED. BOTH INRATIO AND LAB VALUES ARE WITHIN THE CONFIDENCE LIMITS FOR INR TESTING. THE RESULTS ARE NOT CONSIDERED DISCREPANT WITHIN THE CONTEXT OF THE DOCUMENTED VARIABILITY FOR INR TESTING. THEREFORE FURTHER TESTING IS NOT REQUIRED AT THIS TIME. INRATIO PRECISION DATA PROVIDED BY END-USER LOT 060736: FIRST TEST INR = 5.4 SECOND TEST INR = 4.3 THIRD TEST = 5.0 MEAN = 4.90; SD = 0.56; %CV = 11.4%. THE %CV IS LESS THAN OR EQUAL TO 20%. PER INTERNAL PROCEDURE, TR 0150, THE PRECISION PASSES THE CRITERIA FOR PRECISION. THE TEST IS CONSIDERED PRECISE AND NO FURTHER TESTING IS REQUIRED AT THIS TIME.

    Description of Event or Problem · 1

    CALLER ALLEGED INACCURACY WITH INRATIO. RESULTS AS FOLLOWS: DATE 2007, INRATIO 5.4, LAB 3.5. DATE SAME DAY, INRATIO 4.3, LAB 3.5. DATE SAME DAY, INRATIO 5.0, LAB 3.5. CALLER ALLEGED IMPRECISION WITH INRATIO. RESULTS AS FOLLOWS: FIRST TEST INR = 5.4, SECOND TEST INR = 4.3, THIRD TEST = 5.0.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST JPA HEMOSENSE, INC. * 060736

    Patients

    Seq Age Sex Outcome Treatment
    1 *