BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SYMBIQ SINGLE CHENNEL

    MDR report key: 3882712 · Received April 10, 2014

    Report

    Report Number
    9615050-2014-02577
    Event Type
    Malfunction
    Date Received
    April 10, 2014
    Date of Event
    March 11, 2014
    Report Date
    March 11, 2014
    Manufacturer
    HOSPIRA COSTA RICA LTD.
    Product Code
    FRN
    PMA / PMN Number
    K110901
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Additional Manufacturer Narrative · 1

    INITIALLY THE DEVICE PASSED TESTING BY NOT ALARMING WITH A S233 MALFUNCTION ALARM CODE. DURING FURTHER TESTING, THE DEVICE COOLING FAN WAS NOTED TO HAVE A ABNORMAL NOISE AND NOT TURNING AS EXPECTED. DURING A REVIEW OF THE DEVICE HISTORY, A S233 MALFUNCTION ALARM CODE WAS NOTED. THE PROBABLE CAUSE OF THE CUSTOMER REPORTED S233 ALARM CODE WAS A BROKEN COOLING FAN. THIS REPORT REPRESENTS ALL THE INFO KNOWN BY THE REPORTER UPON QUERY BY HOSPIRA PERSONNEL.

    Description of Event or Problem · 1

    THE CUSTOMER CONTACT REPORTED DURING PREVENTIVE MAINTENANCE TESTING AT THE USER FACILITY, THE DEVICE ALARMED WITH A S233 (OVER TEMPERATURE ERROR) MALFUNCTION ALARM CODE. THERE WERE NO REPORTS OF ANY ADVERSE PT EVENTS AND NO REPORTED DELAYS OF CRITICAL THERAPIES WHILE THE DEVICE WAS IN CLINICAL USE. NO ADD'L INFO WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    216341 SYMBIQ SINGLE CHENNEL 80FRN FRN HOSPIRA COSTA RICA LTD. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA