BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENTERAL FEEDING TUBE

    MDR report key: 5055947 · Received September 4, 2015

    Report

    Report Number
    5055947
    Event Type
    Injury
    Date Received
    September 4, 2015
    Date of Event
    August 9, 2015
    Report Date
    August 12, 2015
    Manufacturer
    CORPAK MEDSYSTEMS
    Product Code
    KNT
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    NJT HAD HOLE IN IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    587947 ENTERAL FEEDING TUBE KNT CORPAK MEDSYSTEMS

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization