BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RYMED IN VISION NEEDLELESS IV CONNECTOR

    MDR report key: 23512084 · Received November 10, 2025

    Report

    Report Number
    MW5178705
    Event Type
    Malfunction
    Date Received
    November 10, 2025
    Date of Event
    October 30, 2025
    Report Date
    October 31, 2025
    Manufacturer
    RYMED TECHNOLOGIES, LLC.
    Product Code
    FPA
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    RYMED IN VISION PLUS NEEDLESS CONNECTOR SET; PART OF THE CONNECTOR BROKE OF (ALMOST LIKE MELTED) DURING PATIENT USE. THIS WAS NOTED WHEN THE RN DISCONNECTED THE CONTRAST TUBING FROM THE IV CONNECTOR. A STUCK-ON FEELING MADE THE NURSE LOOK CLOSER OF THE CONNECTION. (SPECIFICALLY, THE GREEN PART COVERING THE TIP OF THE LURE LOCK).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1934546 RYMED IN VISION NEEDLELESS IV CONNECTOR SET, ADMINISTRATION, INTRAVASCULAR FPA RYMED TECHNOLOGIES, LLC. C00425

    Patients

    Seq Age Sex Outcome Treatment
    1 28 YR Male