BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCU-GUARD

    MDR report key: 488984 · Received October 8, 2003

    Report

    Report Number
    2183620-2003-00025
    Event Type
    Injury
    Date Received
    October 8, 2003
    Report Date
    September 8, 2003
    Manufacturer
    SYNOVIS SURGICAL INNOVATIONS
    Product Code
    MTZ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IN 2000 (EXACT DATE UNKNWON), PATIENT UNDERWENT ENUCLEATION PROCEDURE FOLLOWED BY IMPLANTATION OF POROUS POLYPROPYLENE ORBITAL PROSTHESIS IMPLANT ALONG WITH OCU-GUARD ORBITAL IMPLANT WRAP. AT TEN WEEKS POST-OP PATIENT PRESENTED WITH 21 MM CONJUNCTIVAL MELT OVER OCU-GUARD WRAP. AT SIX MONTHS POST-OP ORBITAL IMPLANT WAS REMOVED. PATIENT POST-OP STATUS: UNKNOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OCU-GUARD ORBITAL IMPLANT WRAP MTZ SYNOVIS SURGICAL INNOVATIONS UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Required Intervention POROUS POLYPROPYLENE ORBITAL PROSTHESIS.