BEUDAMED
    FDA Adverse Event Other Summary report: N

    KNIFE BLADE

    MDR report key: 20692 · Received March 1, 1995

    Report

    Report Number
    20692
    Event Type
    Other
    Date Received
    March 1, 1995
    Date of Event
    December 29, 1994
    Report Date
    March 1, 1995
    Manufacturer
    MILTEX INSTRUMENT CO., INC.
    Product Code
    GES
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING TOTAL KNEE PROCEDURE, #10 KNIFE BLADE BROKE WHILE SURGEON DISSECTING TISSUE WITHIN KNEE. ALL PIECES ACCOUNTED FOR. NO PT INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KNIFE BLADE KNIFE BLADE GES MILTEX INSTRUMENT CO., INC. #10

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Other