BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIFECARE PLUM

    MDR report key: 1113083 · Received August 1, 2008

    Report

    Report Number
    1113083
    Event Type
    Malfunction
    Date Received
    August 1, 2008
    Date of Event
    June 14, 2008
    Report Date
    July 28, 2008
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    TN, US

    Narratives

    Description of Event or Problem · 1

    PLUM PUMP HAD A MALFUNCTION CODE OF E24. RN TOOK PUMP OUT OF SERVICE AND TAGGED IT. AN ERROR E24 INDICATES A PROBLEM WITH THE BATTERY. THE BATTERY WAS REPLACED AND THE PUMP RETESTED. THE PUMP CHECKED OUT TO BE OKAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIFECARE PLUM PUMP, IV FRN ABBOTT LABORATORIES, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR