BEUDAMED
    FDA Adverse Event Other Summary report: N

    BIOPRO DIGITAL COMPRESSION SCREW

    MDR report key: 573731 · Received February 2, 2005

    Report

    Report Number
    1833506-2005-00002
    Event Type
    Other
    Date Received
    February 2, 2005
    Date of Event
    November 25, 2004
    Report Date
    January 31, 2005
    Manufacturer
    BIOPRO, INC.
    Product Code
    JDW
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PATIENT TREATED FOR HAMMERTOE. DC SURGICAL SCREW IMPLANTED. SCREW BROKE WHILE PATIENT WAS WALKING IN NORMAL SHOE 5 WEEKS POST OP. NO INJURY OCCURRED TO PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOPRO DIGITAL COMPRESSION SCREW THREADED FIXATION PIN JDW BIOPRO, INC. 17114 M097050

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other