BEUDAMED
    FDA Adverse Event Death Summary report: N

    CORTRAK 2 ENTERAL ACCESS SYSTEM

    MDR report key: 20226926 · Received September 13, 2024

    Report

    Report Number
    MW5159602
    Event Type
    Death
    Date Received
    September 13, 2024
    Date of Event
    August 3, 2024
    Report Date
    September 11, 2024
    Manufacturer
    AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)
    Product Code
    KNT
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    CORTRAK CAUSE PNEUMOTHORAX IN GENTLEMAN. CHEST TUBE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1553893 CORTRAK 2 ENTERAL ACCESS SYSTEM TUBES, GASTROINTESTINAL (AND ACCESSORIES) KNT AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.) 20-0950

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR Male Death