Retiro De Equipo (Recall) de Cemented tibial bases size 3

Según L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en France que fue producido por Depuy.

¿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
    Recall
  • Fecha
    2006-11-28
  • País del evento
  • Fuente del evento
    ANSM
  • URL de la fuente del evento
  • Notas / Alertas
    French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 France.
  • Notas adicionales en la data
  • Acción
    DEPUY company has withdrawn from the market on November 23, 2006 all batches of references 149823003 and 149824003 of the medical device called "cemented tibial bases size 3 - Unicompartimentale Preservation range" following difficulties of assembly of the polyethylene insert in the base tibial. No post-operative disassembly incidents have been reported to date in the world. The company has directly notified the recipients of the offending references with the attached message (23/11/2006) (28 KB) validated by the Afssaps .. This information is addressed to the directors of health establishments and the local correspondents of materiovigilance for diffusion, if necessary with the services concerned (surgeons, supervisors of blocks) .. The competent European authorities concerned are informed of this measurement by the manufacturer.

Device

  • Modelo / Serial
  • Descripción del producto
    medical_device
  • Manufacturer

Manufacturer