BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BHR

    MDR report key: 2771530 · Received October 4, 2012

    Report

    Report Number
    3005477969-2012-00317
    Event Type
    Injury
    Date Received
    October 4, 2012
    Report Date
    October 4, 2012
    Manufacturer
    SMITH & NEPHEW ORTHOPAEDICS, LTD.
    Product Code
    NXT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A REVISION SURGERY IS PLANNED FOR (B)(6), 2012 TO CORRECT A LEG LENGTH DISCREPANCY WHICH OCCURRED AFTER HIP REPLACEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BHR ACETABULAR CUP NXT SMITH & NEPHEW ORTHOPAEDICS, LTD.

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R FEMORAL HEAD, PART AND LOT# UNKNOWN| FEMORAL STEM, PART AND LOT# UNKNOWN