BEUDAMED
    FDA Adverse Event Other Summary report: N

    IRIS SCISSORS

    MDR report key: 13918 · Received June 10, 1994

    Report

    Report Number
    MW1002430
    Event Type
    Other
    Date Received
    June 10, 1994
    Date of Event
    April 27, 1994
    Report Date
    May 23, 1994
    Manufacturer
    AESCULAP CORP.
    Product Code
    HNF
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INTRAOPERATIVELY, AS THE INSTRUMENTS WERE BEING CLEANED, IT WAS NOTED THAT THE TIP OF THE CURVED SHARP IRIS SCISSORS HAD BROKEN LEAVING A SEGMENT APPROX 2-3 MM LONG AND 1-2 MM WIDE ABOVE THE BONY DORSUM. DUE TO THE LOCATION OF THE SCISSOR TIP, THE SURGEON ELECTED TO LEAVE IT IN THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IRIS SCISSORS IRIS SCISSORS HNF AESCULAP CORP. BC 211 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 38 YR Other