BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COBAS INTEGRA 400

    MDR report key: 1052527 · Received May 22, 2008

    Report

    Report Number
    1823260-2008-04254
    Event Type
    Malfunction
    Date Received
    May 22, 2008
    Date of Event
    May 3, 2008
    Report Date
    May 22, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    JJE
    PMA / PMN Number
    K951595
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    ONE PATIENT WITH DISCREPANT SODIUM RESULTS. INITIAL RESULT 140.6 MMOL/L, REPEAT 131 MMOL/L (DIFFERENT ANALYZER, ALTERNATE METHODOLOGY). THE INITIAL RESULT WAS NOT REPORTED. THE FIELD SERVICE REP DETERMINED THE MIX TOWER TO BE THE CAUSE AND HE REPLACED THE MIXTOWER. PERFORMANCE TESTS PERFORMED WHICH WERE WITHIN SPECIFICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COBAS INTEGRA 400 CLINICAL CHEMISTRY ANALYZER - JJE JJE ROCHE DIAGNOSTICS I400

    Patients

    Seq Age Sex Outcome Treatment
    1 87 YR