BEUDAMED
    FDA Adverse Event Summary report: N

    ETHICON

    MDR report key: 3008611 · Received March 6, 2008

    Report

    Report Number
    3008611
    Date Received
    March 6, 2008
    Date of Event
    February 22, 2008
    Report Date
    March 3, 2008
    Manufacturer
    ETHICON ENDOSURGERY, INC
    Product Code
    FZT
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PER SURGEON - 3 DIFFERENT CUTTERS USED AND EACH DID NOT WORK PROPERLY PER DR. (B)(4): LOT # D4JX78 - EXP 11/2012, LOT # D4JP70 - EXP 10/2012, LOT # D4JP04 - EXP 10/2012.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ETHICON ENDOPATH ARTICULATING CUTTER FZT ETHICON ENDOSURGERY, INC

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR