BEUDAMED
    FDA Adverse Event Other Summary report: N

    BIOMET

    MDR report key: 2213811 · Received June 26, 2007

    Report

    Report Number
    MW5021742
    Event Type
    Other
    Date Received
    June 26, 2007
    Date of Event
    May 18, 2007
    Report Date
    June 26, 2007
    Manufacturer
    BIOMET
    Product Code
    JWH
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    COMPLAINTS OF RIGHT KNEE PAIN - LOOSE PATELLAR. COMPONENT REPAIRED. XRAY - SUBLUXATION OF PATELLAR BUTTON. NO SIGNS & SYMPTOMS OF SEPSIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOMET PATTELLA IMPLANT JWH BIOMET

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR