BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONTOUR CURVED CUTTER STAPLER

    MDR report key: 842157 · Received April 17, 2007

    Report

    Report Number
    1527736-2007-02785
    Event Type
    Injury
    Date Received
    April 17, 2007
    Date of Event
    March 6, 2007
    Report Date
    March 27, 2007
    Manufacturer
    ETHICON ENDO SURGERY, INC. (CINCINNATI)
    Product Code
    GDW
    PMA / PMN Number
    K040038
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    IN A CONVERSATION WITH THE DIR OF RISK MGMT ON 4/16/2007, SHE STATED THE PT WAS FINE. THERE WAS NO FURTHER INFO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONTOUR CURVED CUTTER STAPLER GDW GDW ETHICON ENDO SURGERY, INC. (CINCINNATI) NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *