BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COOL PATH DUO 7F, 1304-CP2-7-1.5(5)-L1-TE4BE1AB

    MDR report key: 2021324 · Received February 8, 2011

    Report

    Report Number
    2030404-2011-00035
    Event Type
    Malfunction
    Date Received
    February 8, 2011
    Date of Event
    January 12, 2011
    Report Date
    January 14, 2011
    Manufacturer
    ST. JUDE MEDICAL, IRVINE
    Product Code
    OAD
    PMA / PMN Number
    P060019
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    WE ARE IN THE PROCESS OF INVESTIGATING THIS DEVICE. WHEN OUR INVESTIGATION HAS BEEN COMPLETED, A F/U REPORT WILL BE SUBMITTED. (B)(4).

    Description of Event or Problem · 1

    PRELIMINARY INVESTIGATION OF A CATHETER RETURNED DUE TO REPORTED OCCLUSION, REVEALED A BROKEN FLUID LUMEN AND LEAKING AT THE HANDLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COOL PATH DUO 7F, 1304-CP2-7-1.5(5)-L1-TE4BE1AB NONE OAD ST. JUDE MEDICAL, IRVINE 83565 3198425

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK