BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INTERMEDICS ORTHOPEDICS-SULZER

    MDR report key: 373947 · Received January 24, 2002

    Report

    Report Number
    MW1023887
    Event Type
    Malfunction
    Date Received
    January 24, 2002
    Date of Event
    August 23, 2001
    Report Date
    January 15, 2002
    Manufacturer
    INTERMEDICS ORTHOPEDICS-SULZER
    Product Code
    JWH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PROSTHESIS WAS RECALLED BY MFR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INTERMEDICS ORTHOPEDICS-SULZER KNEE COMPONENTS JWH INTERMEDICS ORTHOPEDICS-SULZER * *

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Other