BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SECUREPORT IV CATHETER SECUREMENT ADHESIVE

    MDR report key: 24649285 · Received March 20, 2026

    Report

    Report Number
    MW5185461
    Event Type
    Injury
    Date Received
    March 20, 2026
    Date of Event
    March 15, 2026
    Report Date
    March 16, 2026
    Manufacturer
    H.B. FULLER MEDICAL ADHESIVE TECHNOLOGIES, LLC
    Product Code
    NZP
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KS, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    PATIENT MISTAKENLY THOUGHT A VIAL OF SECURE PORT IV ADHESIVE WAS EYE DROPS. SHE OPENED THE PACKAGE AND PUT THE ENTIRE CONTENTS INTO HER EYE. GLUING HER EYE SHUT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    712988 SECUREPORT IV CATHETER SECUREMENT ADHESIVE SEALANT, MICROBIAL NZP H.B. FULLER MEDICAL ADHESIVE TECHNOLOGIES, LLC 254441

    Patients

    Seq Age Sex Outcome Treatment
    1 25 YR Female Hospitalization