BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BAXTER

    MDR report key: 404511 · Received July 9, 2002

    Report

    Report Number
    MW1025536
    Event Type
    Malfunction
    Date Received
    July 9, 2002
    Date of Event
    June 19, 2002
    Report Date
    June 28, 2002
    Manufacturer
    BAXTER
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    IV PUMP IN USE IN "SCN", HEARD LOUD BEEPING SOUNDS AND SMELLED SULFUR ODOR. PUMP WAS UNPLUGGED AND VERY HOT ON TOP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BAXTER IV PUMP FRN BAXTER "COLLEAUGE" 245641 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *