BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SOLID MALAR IMPLANT

    MDR report key: 224390 · Received May 21, 1999

    Report

    Report Number
    2024601-1999-00092
    Event Type
    Injury
    Date Received
    May 21, 1999
    Date of Event
    April 27, 1999
    Report Date
    April 27, 1999
    Manufacturer
    MCGHAN MEDICAL CORP.
    Product Code
    LZK
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    ALLEGED EXTRUSION AND MULTIPLE VARIED INJURIES. FOLLOW UP FINDINGS: LEGAL CLAIM UNSUBSTANTIATED BY HEALTH CARE PROFESSIONAL. OUTCOME: UNDETERMINED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SOLID MALAR IMPLANT Implant SOLID MALAR IMPLANT LZK MCGHAN MEDICAL CORP. FACIAL NA

    Patients

    Seq Age Sex Outcome Treatment
    1 36 YR Other