BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AXSYM DIGOXIN III

    MDR report key: 1010014 · Received May 11, 2007

    Report

    Report Number
    2623532-2007-00104
    Event Type
    Malfunction
    Date Received
    May 11, 2007
    Date of Event
    March 14, 2007
    Report Date
    April 11, 2007
    Manufacturer
    ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.
    Product Code
    KXT
    PMA / PMN Number
    K061249
    Removal / Correction Number
    2623532-4/10/07-003-C
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IS AN INITIAL REPORT. AN INVESTIGATION IS IN PROCESS. A FINAL REPORT WILL BE SUBMITTED WHEN THE INVESTIGATION IS COMPLETE.

    Description of Event or Problem · 1

    THREE LAB HAVE REPORTED DISCORDANT PT RESULTS TO THE INSTITUTE OF PUBLIC HEALTH FOR THE AXSYM DIGOXIN III ASSAY COMPARED TO THE AXSYM DIGOXIN II ASSAY AND THE ROCHE ELECSYS DIGOXIN METHOD. AXSYM DIGOXIN III VALUES WERE INCREASED UP TO DOUBLE THE VALUES OF THE OTHER METHODS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AXSYM DIGOXIN III MEIA FOR THE MEASUREMENT OF DIGOXIN KXT ABBOTT DIAGNOSTICS INTERNATIONAL, LTD. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NI Other AXSYM ANALYZER LIST # 7A83-93