BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PANDA

    MDR report key: 93922 · Received May 30, 1997

    Report

    Report Number
    MW1011373
    Event Type
    Malfunction
    Date Received
    May 30, 1997
    Date of Event
    May 16, 1997
    Report Date
    May 23, 1997
    Manufacturer
    ELAN PHARMA, INC.
    Product Code
    FPD
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    ME, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ENTERAL FEEDING TUBE WAS INSERTED, BUT HAD TO BE REMOVED BECAUSE STYLET COULD NOT BE WITHDRAWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PANDA Implant ENTERAL FEEDING TUBE FPD ELAN PHARMA, INC. * 96115

    Patients

    Seq Age Sex Outcome Treatment
    1 *