BEUDAMED
    FDA Adverse Event Death Summary report: N

    CONMED CORPORATION

    MDR report key: 291034 · Received August 16, 2000

    Report

    Report Number
    1720159-2000-00060
    Event Type
    Death
    Date Received
    August 16, 2000
    Date of Event
    November 1, 1999
    Report Date
    July 18, 2000
    Manufacturer
    CONMED/ASPEN LABS
    Product Code
    GEI
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE SURGICAL PROCEDURE WAS A UROLOGICAL PROCEDURE. THERE WAS NOT ANY HARM TO THE PT.

    Description of Event or Problem · 1

    THE SURGICAL PROCEDURE WAS A UROLOGICAL PROCEDURE. CONMED/ASPEN LABS HAS BEEN UNABLE TO GET ANY ADDITIONAL INFO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONMED CORPORATION ELECTROSURGICAL UNIT GEI CONMED/ASPEN LABS EXCALIBUR PLUS PC NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death