BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURACATH

    MDR report key: 24303613 · Received February 10, 2026

    Report

    Report Number
    24303613
    Event Type
    Malfunction
    Date Received
    February 10, 2026
    Date of Event
    January 22, 2026
    Report Date
    January 30, 2026
    Manufacturer
    INTERRAD MEDICAL, INC
    Product Code
    LJS
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    UT
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    RN FLUSHING PATIENT TRIPLE LUMEN PICC [PERIPHERALLY INSERTED CENTRAL CATHETER] LINE AND NOTICED IT WAS LEAKING. IT SEEMED TO BE LEAKING FROM THE WHITE LUMEN. THE CHG [CHLORHEXIDINE GLUCONATE] PORTION ON THE DRESSING WAS BUBBLING WITH FLUID AND WAS LEAKING DOWN THE DRESSING. THERE WAS POSITIVE BLOOD RETURN ON ALL THREE LUMENS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    362964 SECURACATH CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS LJS INTERRAD MEDICAL, INC 5F

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Female