BEUDAMED
    FDA Adverse Event Death Summary report: N

    CORTRAK EAS

    MDR report key: 20156754 · Received September 5, 2024

    Report

    Report Number
    MW5159223
    Event Type
    Death
    Date Received
    September 5, 2024
    Date of Event
    August 14, 2024
    Report Date
    September 2, 2024
    Manufacturer
    AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)
    Product Code
    KNT
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AL, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    LUNG PERFORATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1835934 CORTRAK EAS TUBES, GASTROINTESTINAL (AND ACCESSORIES) KNT AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Death