BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BONE BIOPSY SYSTEM

    MDR report key: 87319 · Received April 25, 1997

    Report

    Report Number
    1811755-1997-00036
    Event Type
    Injury
    Date Received
    April 25, 1997
    Manufacturer
    STRYKER INSTRUMENTS
    Product Code
    KNW
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DOCTOR PERFORMING A CORE DECOMPRESSION ON THE FEMUR USING THE 233-797. THE GUIDE WIRE SNAPPED OFF INSIDE THE FEMORAL HEAD. DOING A BIOPSY, HE HAD TO USE A 233-796 TO EXTRACT THE PIECE THAT WAS BROKEN OFF IN THE FEMORAL HEAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BONE BIOPSY SYSTEM BONE BIOPSY SYSTEM KNW STRYKER INSTRUMENTS 0233-700-000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention