BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIFECARE 5000 PLUM

    MDR report key: 740835 · Received June 27, 2006

    Report

    Report Number
    740835
    Event Type
    Other
    Date Received
    June 27, 2006
    Date of Event
    October 23, 2005
    Report Date
    June 27, 2006
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    FRN
    Report Source
    User Facility report
    Reporter Location
    NY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    THE IV PUMP REPORTEDLY DID NOT ALARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIFECARE 5000 PLUM PUMP, IV FRN ABBOTT LABORATORIES, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 6 MO