BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SYMBIQ

    MDR report key: 2081145 · Received April 27, 2011

    Report

    Report Number
    2081145
    Event Type
    Malfunction
    Date Received
    April 27, 2011
    Date of Event
    April 27, 2011
    Report Date
    April 27, 2011
    Manufacturer
    HOSPIRA
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IL, US

    Narratives

    Description of Event or Problem · 1

    IV PUMP WAS TURNED ON, BUT CAME UP WITH THE "WHITE SCREEN OF DEATH", DEVICE MALFUNCTION: SOFTWARE ERROR, PROCNAME: NVRAMACCESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SYMBIQ GENERAL PURPOSE INFUSION PUMP FRN HOSPIRA SYMBIQ *

    Patients

    Seq Age Sex Outcome Treatment
    1 *