Events

Retiro De Equipo (Recall) de Safe access infusion set

Según Pharmaceuticals and Medical Devices Agency, Japan, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Japan que fue producido por Japan Covidien Corporation.

¿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
  • ID del evento
    2-8269
  • Fecha
    2018-07-04
  • País del evento
    Japan
  • Fuente del evento
    PMDAJ
  • URL de la fuente del evento
    http://www.info.pmda.go.jp/rgo/MainServlet?recallno=2-8269
  • Notas / Alertas
    Japanese data is current through August 2018. All of the data comes from the Japanese Pharmaceuticals and Medical Devices Agency, 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 Japan.
  • Notas adicionales en la data

Device

Safe access infusion set
  • Modelo / Serial
  • Descripción del producto
    Natural fall type · Combined use infusion set for pump connection
  • Manufacturer
    Japan Covidien Corporation

Manufacturer

Japan Covidien Corporation
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • 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
    PMDAJ