BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COBAS INTEGRA 800

    MDR report key: 1760842 · Received July 13, 2007

    Report

    Report Number
    1823260-2007-06064
    Event Type
    Malfunction
    Date Received
    July 13, 2007
    Date of Event
    June 22, 2007
    Report Date
    July 13, 2007
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    JJE
    PMA / PMN Number
    K951595
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    INITIAL ALKALINE PHOSPHATASE RESULT OF 212 U/L. SAME SAMPLE REPEATED GAVE RESULT OF 118U/L. SAME SAMPLE REPEATED A THIRD TIME IN A CUP, RECOVERED 117, 116 U/L. INITIAL RESULT WAS NOT REPORTED. THE USER PERFORMED MAINTENANCE AND TROUBLESHOOTING ACTIVITIES WHICH RESOLVED THE ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COBAS INTEGRA 800 CLINICAL CHEMISTRY ANALYZER - JJE JJE ROCHE DIAGNOSTICS I800

    Patients

    Seq Age Sex Outcome Treatment
    1 NA