BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 900519 · Received August 20, 2007

    Report

    Report Number
    2954730-2007-00374
    Event Type
    Malfunction
    Date Received
    August 20, 2007
    Date of Event
    July 27, 2007
    Report Date
    August 15, 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 070274: DATE 2007, FIRST TEST INR = 1.7, SECOND TEST INR = 1.8, MEAN = 1.75; SD = 0.08; %CV = 4.04%. DATE 2007, FIRST TEST INR = 2.3, SECOND TEST INR = 2.1, MEAN = 2.2; SD = 0.14; %CV = 6.43%. THE %CV IS LESS THAN 20% FOR DATA SETS. PER INTERNAL PROCEDURE, THE PRECISION PASSES THE CRITERIA FOR PRECISION. THE TEST IS CONSIDERED PRECISE AND NO FURTHER TESTING IS REQUIRED AT THIS TIME. DISCREPANT RESULTS (ACCURACY) COMPARISON OF INRATIO TEST WITH LAB RESULTS PROVIDED BY END-USER AT TIME COMPLAINT WAS FILED: 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.

    Description of Event or Problem · 1

    CALLER ALLEGES IMPRECISION WITH INRATIO. RESULTS AS FOLLOWS: FIRST TEST INR = 1.7, SECOND TEST INR = 1.8; FIRST TEST INR = 2.3, SECOND TEST INR = 2.1. CALLER ALLEGES INACCURACY WITH INRATIO RESULTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST JPA HEMOSENSE, INC. 070274

    Patients

    Seq Age Sex Outcome Treatment
    1 YR