Retiro De Equipo (Recall) de MSA Hip SystemMSA Neutral Femoral Neck

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Global Manufacturing Technology Pty Ltd.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
  • ID del evento
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
  • País del evento
  • Fuente del evento
  • URL de la fuente del evento
  • Notas / Alertas
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • Notas adicionales en la data
  • Causa
    The 2013 annual report of the national joint replacement registry (njrr) indicates that up to december 2012, the cumulative percent revision of the msa hip system has been calculated as 6.2 % at one year and approximately 11% at 2 years , both of which are significantly higher than that of other hip replacement prostheses. the most common reasons for revision of msa to date have been loosening/lysis and peri-prosthetic fracture, but there have also been a few revisions due to prosthesis dislocation, pain and infection.After consultation with the therapeutic goods administration, a decision has been made by global orthopaedic technology to cease supply of the msa hip stem. this device has been removed from the australian register of therapeutic goods.
  • Acción
    Global Orthopaedic Technology is informing implanting surgeons that it is advisable for annual clinical and radiological examinations to be performed on patients who have been implanted with this device, in accordance with routine patient post arthroplasty care. For more details, please see .


  • Modelo / Serial
    MSA Hip SystemMSA Neutral Femoral Neck Catalogue number range: GH-220-00 to GH-260-08MSA Ante-Retro-Version Femoral Neck Catalogue number range: GH-221-00 to GH-261-00MSA Titanium HA Custom Femoral Stem Catalogue number range: GH-1400-00 to GH-14000-25ARTG Number: 120787
  • Manufacturer