Alerta De Seguridad para Silimed medical devices (all - including breast implants)

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Silimed.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • Fecha
    2015-09-25
  • Fecha de publicación del evento
    2015-09-25
  • País del evento
  • Fuente del evento
    DH
  • URL de la fuente del evento
  • Notas / Alertas
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: silimed medical devices (all - including breast implants) the therapeutic goods administration (tga) of australia posted a medical device safety alert concerning all medical devices manufactured by silimed. the tga is aware that european union (eu) health regulators have suspended approval for all devices manufactured by the brazilian company silimed following an inspection of a manufacturing site. silimed's ce certificate was suspended after german health officials inspected silimed's manufacturing plant and found that the surfaces of some devices were contaminated with unknown particles. in general, a medical device cannot be marketed in europe without carrying a ce mark of conformity. as a precautionary measure and in consultation with the tga, the australian distributor has been contacting surgeons who have been supplied with these implants to recommend any planned implant surgeries be postponed. the tga has had no adverse event reports relating to these products and there has been no indication that these issues would pose a threat to the implanted person's safety. for details, please refer to the following link:http://www.Tga.Gov.Au/alert/silimed-medical-devices-all-including-breast-implants if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 25 september 2015.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Silimed medical devices (all - including breast implants)
  • Manufacturer

Manufacturer