BEUDAMED
    FDA Adverse Event Injury Summary report: N

    R3

    MDR report key: 3811393 · Received May 15, 2014

    Report

    Report Number
    3005477969-2014-00327
    Event Type
    Injury
    Date Received
    May 15, 2014
    Date of Event
    February 21, 2012
    Report Date
    May 14, 2014
    Manufacturer
    SMITH & NEPHEW ORTHOPAEDICS LTD
    Product Code
    NXT
    PMA / PMN Number
    P040033
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED DUE TO FAILURE OF THE IMPLANTS. THE TYPE OF FAILURE WAS NOT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    291333 R3 COCR ACETABULAR LINER NXT SMITH & NEPHEW ORTHOPAEDICS LTD

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R FEMORAL STEM, PART AND LOT NUMBERS UNKNOWN| ACETABULAR SHELL, PART AND LOT NUMBERS UNKNOWN