BEUDAMED
    FDA Adverse Event Death Summary report: N

    CORPAK FEEDING TUBE

    MDR report key: 24271095 · Received February 5, 2026

    Report

    Report Number
    MW5183424
    Event Type
    Death
    Date Received
    February 5, 2026
    Date of Event
    August 14, 2025
    Report Date
    January 30, 2026
    Manufacturer
    AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)
    Product Code
    KNT
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    CORPAK FEEDING TUBE WAS KINKED AT (B)(6). THEY PULLED ON IT BUT DID NOT REMOVE RESULTING IN A DOUBLE KINK, CAUSED REFEEDING SYNDROME. ON (B)(6) 2025 TUBE WAS REMOVED BUT (B)(6) DID NOT BALANCE ELECTROLYTES AND DISCHARGED THE PATIENT. PATIENT DIED 3 DAYS LATER FROM SUDDEN CARDIAC ARREST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    330905 CORPAK FEEDING TUBE TUBES, GASTROINTESTINAL (AND ACCESSORIES) KNT AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Female Death DIURETICS.| LACTULOSE.| VITAMINS.