Events

Notificaciones De Seguridad De Campo acerca de Sports Medicine and Trauma Products

Según Turkey Drugs and Medical Devices Agency (Titck), este evento ( notificaciones de seguridad de campo ) involucró a un dispositivo médico en Turkey que fue producido por Biomet Sports Medicine and Trauma.

¿Qué es esto?

Las notificaciones de seguridad de campo son comunicaciones sobre acciones que se pueden estar tomando en relación con un producto que se encuentra en el mercado, enviadas por los fabricantes de dispositivos médicos o sus representantes. Estas notificaciones son principalmente para trabajadores de la salud, pero también para usuarios. Pueden incluir alertas y retiro de equipos.

Más información acerca de la data acá
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/361 & HHE 15-20
  • Fecha
    2016-04-22
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817041706/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-361%20SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data

Device

Sports Medicine and Trauma Products

Manufacturer

Biomet Sports Medicine and Trauma
  • Empresa matriz del fabricante (2017)
    Zimmer Biomet Holdings
  • Comentario del fabricante
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    TDMDAT