BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NEW LIGASURE 5MM

    MDR report key: 3983910 · Received June 24, 2014

    Report

    Report Number
    1717344-2014-00539
    Event Type
    Malfunction
    Date Received
    June 24, 2014
    Date of Event
    March 14, 2014
    Report Date
    June 2, 2014
    Manufacturer
    COVIDIEN LP
    Product Code
    GEI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE SAMPLE HAS BEEN REQUESTED BUT TO DATE THE INCIDENT SAMPLE HAS NOT BEEN RECEIVED FOR EVALUATION. IF THE SAMPLE IS RECEIVED OR IF ADDITIONAL INFORMATION PERTINENT TO THE INCIDENT IS OBTAINED A FOLLOW-UP REPORT WILL BE SUBMITTED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT BLEEDING OCCURRED AFTER MESENTERY VESSELS WERE SEALED DURING A RIGHT HEMI COLECTOMY. THE BLEEDING WAS DESCRIBED AS "NOT SIGNIFICANT". ANOTHER LIGASURE DEVICE WAS USED TO COMPLETE THE PROCEDURE AND THERE WAS NO INJURY TO THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    368483 NEW LIGASURE 5MM LIGASURE VESSEL SEALING SYSTEM GEI COVIDIEN LP 254767X

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK