BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DIMENSION (R) CLINICAL CHEMISTRY SYSTEM

    MDR report key: 1962516 · Received January 18, 2011

    Report

    Report Number
    2517506-2011-00006
    Event Type
    Malfunction
    Date Received
    January 18, 2011
    Date of Event
    January 3, 2011
    Report Date
    January 5, 2011
    Manufacturer
    SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW
    Product Code
    MMI
    PMA / PMN Number
    K010313
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    MEDICAL TECHNOLOGIST

    Narratives

    Additional Manufacturer Narrative · 1

    ANALYSIS OF THE INSTRUMENT AND INSTRUMENT DATA INDICATE THAT THE CAUSE FOR THE FALSELY ELEVATED TROPONIN I RESULT IS UNKNOWN. THE INSTRUMENT IS PERFORMING WITHIN SPECIFICATIONS. NO FURTHER EVALUATION OF THE DEVICE IS REQUIRED.

    Description of Event or Problem · 1

    A FALSELY ELEVATED TROPONIN I RESULT WAS OBTAINED ON A PATIENT SAMPLE. THE RESULT WAS NOT REPORTED TO THE PHYSICIAN. THE SAMPLE WAS REPEATED AN THE SAME INSTRUMENT AND A NEGATIVE RESULT WAS OBTAINED. THE NEGATIVE RESULT WAS REPORTED. PATIENT TREATMENT WAS NOT REPORTED TO HAVE BEEN ALTERED OR PRESCRIBED. THERE WAS NO REPORT OF ADVERSE HEALTH CONSEQUENCES AS A RESULT OF THE FALSELY ELEVATED TROPONIN I RESULT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DIMENSION (R) CLINICAL CHEMISTRY SYSTEM TROPONIN I FLEX(R) REAGENT CARTRIDGE MMI SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW RXL MAX FB1258

    Patients

    Seq Age Sex Outcome Treatment
    1