BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TELEFLEX MEDICAL

    MDR report key: 8523311 · Received April 12, 2019

    Report

    Report Number
    8523311
    Event Type
    Injury
    Date Received
    April 12, 2019
    Date of Event
    March 30, 2019
    Report Date
    April 10, 2019
    Manufacturer
    TELEFLEX
    Product Code
    CAZ
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    EPIDURAL CATHETER WOULD NOT COME OUT. ANESTHESIOLOGISTS MADE SEVERAL ATTEMPTS. PT WAS TRANSFERRED TO ANOTHER FACILITY FOR SURGICAL REMOVAL. IT WAS FOUND TO BE A TRUE KNOT WHICH IS VERY RARE BUT CAN HAPPEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    305072 TELEFLEX MEDICAL EPIDURAL CATHETER CAZ TELEFLEX

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Hospitalization