BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SULZER MEDICA

    MDR report key: 313058 · Received January 17, 2001

    Report

    Report Number
    MW1020855
    Event Type
    Injury
    Date Received
    January 17, 2001
    Date of Event
    January 16, 2001
    Report Date
    January 17, 2001
    Manufacturer
    SULZER MEDICA
    Product Code
    KWB
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT RECEIVED A SULZERMEDICA HIP IMPLANT THAT WAS RECALLED BY THE CO IN A NATIONWIDE RECALL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2000 SULZER MEDICA HIP - ACETABULAR SHELLS KWB SULZER MEDICA * *

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Other| R