BEUDAMED
    FDA Adverse Event Summary report: N

    CANNULA AND OBTURATOR

    MDR report key: 1061705 · Received June 10, 2008

    Report

    Report Number
    1061705
    Date Received
    June 10, 2008
    Date of Event
    May 30, 2008
    Report Date
    June 10, 2008
    Manufacturer
    SMITH & NEPHEW, INC.
    Product Code
    NBH
    Report Source
    User Facility report
    Reporter Location
    RI, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    ARTHROSCOPIC PROCEDURE WITH 1.9 SHORT SCOPE SET. DURING PROCEDURE IT WAS NOTED THAT THERE WERE METAL SHAVINGS IN THE PATIENT'S JOINT POSSIBLY FROM INNER CANNULA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CANNULA AND OBTURATOR CANNULA AND OBTURATOR NBH SMITH & NEPHEW, INC. NOT KNOWN 50139928 & 50243093

    Patients

    Seq Age Sex Outcome Treatment
    1 38 YR