BEUDAMED
    FDA Adverse Event Other Summary report: N

    ENDOPATH ELECTROSURGERY PROBE PLUS II

    MDR report key: 12363 · Received March 29, 1994

    Report

    Report Number
    MW1001286
    Event Type
    Other
    Date Received
    March 29, 1994
    Date of Event
    March 16, 1994
    Report Date
    March 17, 1994
    Manufacturer
    ETHICON ENDOSURGERY
    Product Code
    FEH
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    SURGEON HAD A DISPOSABLE PROBE INSIDE A TROCAR IN A PT'S ABDOMEN, WHEN THE PROBE SPONTANEOUSLY TURNED ON WITHOUT CONTROL OF THE DR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENDOPATH ELECTROSURGERY PROBE PLUS II CAUTERY/IRRIGATION/SUCTION FEH ETHICON ENDOSURGERY EPS04

    Patients

    Seq Age Sex Outcome Treatment
    1 20 YR Other BOVIE/VALLEY LAB # LAC 18399L-20