BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CLEARLINK/CONTINU-FLO/DUO-VENT

    MDR report key: 23423811 · Received October 30, 2025

    Report

    Report Number
    23423811
    Event Type
    Malfunction
    Date Received
    October 30, 2025
    Date of Event
    October 7, 2025
    Report Date
    October 9, 2025
    Manufacturer
    BAXTER HEALTHCARE CORPORATION.
    Product Code
    FPA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MO
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IV PRIMARY TUBING CLEARLINK FLO LOT (10) R@%D@1208 01 00085412071107 EXP. 2027-04-21 THIS IV TUBING WAS ATTACHED TO IV ANTIBIOTIC AND TUBING CAME APART AT THE MIDWAY POINT OF TUBING AND ALL OF THE IV ANTIBIOTIC SPILLED INTO THE SINK IN THE MEDICATION ROOM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1370563 CLEARLINK/CONTINU-FLO/DUO-VENT SET, ADMINISTRATION, INTRAVASCULAR FPA BAXTER HEALTHCARE CORPORATION. 2C8541

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown