BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MIC J TUBE

    MDR report key: 24234109 · Received February 2, 2026

    Report

    Report Number
    MW5183133
    Event Type
    Malfunction
    Date Received
    February 2, 2026
    Date of Event
    December 22, 2025
    Report Date
    December 27, 2025
    Manufacturer
    AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)
    Product Code
    KNT
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    NURSE
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PATIENT HAD A GJ(GASTRO-JEJUNAL) TUBE PLACED ON (B)(6) 2025. IT WAS DISCOVERED AFTER THE PLACEMENT OF THE TUBE THAT THE TUBE WAS NOT HOLDING WATER TO KEEP THE TUBE FROM COMING DISPLACED. PATIENT RETURNED TO THE OPERATING ROOM TO HAVE THE TUBE REPLACED DUE TO THE DEFECTIVE TUBE. SPECIAL NEEDS PATIENT WHO HAS CHRONIC GJ TUBE FOR ASPIRATION RISK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    303541 MIC J TUBE TUBES, GASTROINTESTINAL (AND ACCESSORIES) KNT AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Female Other