BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DLP

    MDR report key: 238477 · Received September 1, 1999

    Report

    Report Number
    MW1017095
    Event Type
    Injury
    Date Received
    September 1, 1999
    Date of Event
    August 27, 1999
    Report Date
    September 1, 1999
    Manufacturer
    DLP, INC.
    Product Code
    DYG
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    PHYSICIAN ATTEMPTED TO REMOVE RIGHT ATRIAL LINE, BUT MET RESISTANCE. HE RE-ATTEMPTED WITH SIMILAR PRESSURE AND THE LINE SNAPPED, LEAVING APPROXIMATELY 13 CM OF CATHETER IN THE BODY. THE PT WAS SENT TO THE CARDIAC CATHETERIZATION ROOM FOR RETRIEVAL OF THE REMAINING PORTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DLP TRANSTHORACIC LINE DYG DLP, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 7 MO Required Intervention