BEUDAMED
    FDA Adverse Event Other Summary report: N

    ADVIA CENTAUR TROPONIN ULTRA ASSAY

    MDR report key: 1220559 · Received October 30, 2008

    Report

    Report Number
    1219913-2008-00082
    Event Type
    Other
    Date Received
    October 30, 2008
    Date of Event
    September 24, 2008
    Report Date
    September 25, 2008
    Manufacturer
    SIEMENS HEALTHCARE DIAGNOSTICS, INC
    Product Code
    MMI
    PMA / PMN Number
    K053020
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    ANALYSIS OF THE INSTRUMENT DATA INDICATE THAT THE CAUSE FOR THE DISCORDANT TROPONIN ULTRA RESULT IS UNKNOWN. NO FURTHER EVALUATION OF THE DEVICE IS REQUIRED.

    Description of Event or Problem · 1

    A POSITIVE ADVIA CENTAUR TROPONIN ULTRA PATIENT RESULT WAS REPORTED TO THE PHYSICIAN. THE PHYSICIAN WAS CONTACTED LATER WHEN THE CKMB RESULTS ON THE SAME PATIENT WERE NORMAL. THE PATIENT SAMPLE WAS RETESTED FOR TROPONIN ULTRA AND THE RETEST RESULTS WERE NEGATIVE. PATIENT TREATMENT WAS NOT ALTERED OR PRESCRIBED. THERE WAS NO REPORT OF ADVERSE HEALTH CONSEQUENCES DUE TO THE DISCORDANT TROPONIN ULTRA RESULT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVIA CENTAUR TROPONIN ULTRA ASSAY TROPONIN IMMUNOASSAY MMI SIEMENS HEALTHCARE DIAGNOSTICS, INC NA 27

    Patients

    Seq Age Sex Outcome Treatment
    1