BEUDAMED
    FDA Adverse Event Other Summary report: N

    BIOMET

    MDR report key: 296176 · Received September 12, 2000

    Report

    Report Number
    MW1019915
    Event Type
    Other
    Date Received
    September 12, 2000
    Date of Event
    September 7, 2000
    Report Date
    September 12, 2000
    Manufacturer
    BIOMET
    Product Code
    HTG
    Report Source
    Voluntary report
    Reporter Location
    AL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    TOTAL LEFT KNEE REPLACEMENT IN 1999. PATELLA BROKE AND WAS REMOVED IN 2000. UNKNOWN IF DEFECTIVE OR DAMAGED AFTER IMPLANTATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOMET PATELLA BUTTON HTG BIOMET * 410380

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Other