BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BIOMET, INC.

    MDR report key: 437913 · Received January 14, 2003

    Report

    Report Number
    437913
    Event Type
    Injury
    Date Received
    January 14, 2003
    Date of Event
    November 6, 2002
    Report Date
    December 6, 2002
    Manufacturer
    BIOMET, INC.
    Product Code
    JWH
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    OK, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    RIGHT KNEE HARDWARE WAS REMOVED DUE TO PAIN, LACK OF RANGE OF MOTION AND MEDIAL COLLATERAL INSUFFICIENCY. DETAILS ON PRODUCT NOT AVAILABLE; FROM ANOTHER FACILITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOMET, INC. KNEE IMPLANTS JWH BIOMET, INC. NA *

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Hospitalization