Retiro De Equipo (Recall) de ENDOTRACHEAL TUBE

Según Health Canada (via FOI), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Canada que fue producido por MEDTRONIC OF CANADA 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
  • Fecha de inicio del evento
  • País del evento
  • Fuente del evento
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
  • Causa
    Medtronic has received complaint reports of "wire through lumen" "cuff leakage" or some variation where a wire was found out of place or to have penetrated the channel wall. most of these reports do not indicate patient injury or adverse health consequences. therefore and to ensure patient safety and out of an abundance of caution medtronic is providing a technical bulletin to reinforce and remind customers of the proper handling of the tube during intubation appropriate warnings and precautions that could relate to the complaints and that are included in the instructions for use (ifu).


  • Modelo / Serial
    Model Catalog: 8229308 (Lot serial: All Lots); Model Catalog: 8229306 (Lot serial: All Lots); Model Catalog: 8229506 (Lot serial: All Lots); Model Catalog: 8229507 (Lot serial: All Lots); Model Catalog: 8229508 (Lot serial: All Lots); Model Catalog: 8229307 (Lot serial: All Lots)
  • Descripción del producto
  • Manufacturer


  • Dirección del fabricante
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source