BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BAXTER

    MDR report key: 1233284 · Received November 7, 2008

    Report

    Report Number
    1233284
    Event Type
    Malfunction
    Date Received
    November 7, 2008
    Date of Event
    October 31, 2008
    Report Date
    November 7, 2008
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US

    Narratives

    Description of Event or Problem · 1

    THE PUMP TRANSFUSING LIPIDS FAILED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BAXTER INFUSION PUMP FRN BAXTER HEALTHCARE CORPORATION * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *