BEUDAMED
    FDA Adverse Event Other Summary report: N

    DUPEN CATHETER

    MDR report key: 14950 · Received March 11, 1994

    Report

    Report Number
    14950
    Event Type
    Other
    Date Received
    March 11, 1994
    Date of Event
    March 8, 1994
    Report Date
    March 11, 1994
    Manufacturer
    C.R. BARD, INC.
    Product Code
    JXG
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    IN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    UPON REMOVAL OF PERMANENT CATHETER, THE TIP REMAINED IN THE PT'S EPIDURAL SPACE DUE TO SHEARING AFTER AN ATTEMPT TO WITHDRAW CATHETER. INITIAL INSERTION OF THE CATHETER WAS 11/93.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DUPEN CATHETER Implant CATHETER JXG C.R. BARD, INC. 36AD1883

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Other