BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 731778 · Received June 23, 2006

    Report

    Report Number
    2954730-2006-00367
    Event Type
    Malfunction
    Date Received
    June 23, 2006
    Date of Event
    June 15, 2006
    Report Date
    June 20, 2006
    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. DATE: 06/14/2006 INRATIO: 4.0, LAB: 3.5, MEAN: 3.75, CONFIDENCE LIMITS: 3.2-5.3, INRATIO:5.2, LAB:3.5, MEAN:4.35, CONFIDENCE LIMITS 2.5-6.5. PER INTERNAL PROCEDURE, THE CALCULATED 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 TME. INRATIO PRESCISION DATA PROVIDED BY END-USER LOT 050726: 06/14/2006 FIRST TEST INR = 4.0 SECOND TEST INR =5.2 MEAN = 4.6; SD =0.85 %CV = 18.4% THE %CV IS LESS THAN OR EQUAL TO 20%. PER INTERNAL PROCEDURE, 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 DISCREPANT RESULTS COMPARED WITH THE LAB. RESULTS AS FOLLOWS: DATE: 06/14/06 ,INRATIO: 4.0, LAB: 3.5, INRATIO:5.2, LAB:3.5. CALLER ALLEGED IMPRECISION WITH INRATIO. RESULTS AS FOLLOWS: 06/14/06 FIRST TEST INR = 4.0 SECOND TEST INR = 5.2

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST JPA HEMOSENSE, INC. * 050726

    Patients

    Seq Age Sex Outcome Treatment
    1