BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDULLARY TUBE

    MDR report key: 216465 · Received March 22, 1999

    Report

    Report Number
    2520274-1999-00009
    Event Type
    Injury
    Date Received
    March 22, 1999
    Date of Event
    February 23, 1999
    Report Date
    February 23, 1999
    Manufacturer
    SYNTHES USA
    Product Code
    FZX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ON FEBRUARY 23, 1999, A MEDULLARY TUBE BROKE IN THE PT'S MEDULLARY CANAL. THE SURGEON HAD TO MAKE AN INCISION AND ENTER THROUGH THE FRACTURE SITE TO RETRIEVE THE PIECES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDULLARY TUBE MEDULLARY TUBE FZX SYNTHES USA NA NI

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Required Intervention