BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HOSPIRA XL "PLUM" IV FLUID

    MDR report key: 1040887 · Received May 12, 2008

    Report

    Report Number
    MW5006806
    Event Type
    Malfunction
    Date Received
    May 12, 2008
    Date of Event
    January 21, 2008
    Report Date
    May 7, 2008
    Manufacturer
    HOSPIRA INC.
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    NURSE THOUGHT THE IV INFUSION PUMP MALFUNCTIONED BY "SUDDENLY PUMPING FLUID FASTER". NO ONE ELSE HAD THE PROBLEM WITH THE PUMP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HOSPIRA XL "PLUM" IV FLUID INFUSION PUMP FRN HOSPIRA INC.

    Patients

    Seq Age Sex Outcome Treatment
    1