BEUDAMED
    FDA Adverse Event Other Summary report: N

    BIOPRO HEMI TOE

    MDR report key: 663929 · Received January 11, 2006

    Report

    Report Number
    1833506-2006-00001
    Event Type
    Other
    Date Received
    January 11, 2006
    Date of Event
    December 1, 2005
    Report Date
    January 6, 2006
    Manufacturer
    BIOPRO, INC.
    Product Code
    KWD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT COMPLAINED THAT TOE WHICH IMPLANT WAS IN WAS LOCKING UP AFTER SURGERY. DOCTOR REMOVED IMPLANT PER PT REQUEST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOPRO HEMI TOE TOE MP JOINT KWD BIOPRO, INC. 10414 M100890

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Required Intervention