BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VHS VARIABLE ANGLE PLATE

    MDR report key: 231206 · Received July 6, 1999

    Report

    Report Number
    1825034-1999-00069
    Event Type
    Injury
    Date Received
    July 6, 1999
    Date of Event
    April 19, 1999
    Report Date
    July 6, 1999
    Manufacturer
    BIOMET, INC.
    Product Code
    HRS
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    VHS COMPRESSION HIP SCREW AND PLATE WERE IMPLANTED IN 1998. HARDWARE WAS EXCHANGED IN 1999, DUE TO NON-UNION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VHS VARIABLE ANGLE PLATE Implant FIXATION, TRAUMA, COMP HRS BIOMET, INC. NA 682890

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention