Alerta De Seguridad para Cereform silicone gel-filled breast implants

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

¿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
    2014-02-24
  • Fecha de publicación del evento
    2014-02-24
  • 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: cereplas cereform silicone gel-filled breast implants the australia therapeutic goods administration (tga) posted a medical device safety alert concerning cereform silicone gel-filled breast implants manufactured by cereplas. the tga was advised on 13 february 2014 that non-implanted cereform silicone gel-filled breast implants have been recalled in france after the french regulatory authority, agence nationale de sécurité du médicament et des produits de santé (ansm), found the sterilisation process used in the manufacture of these devices had not been fully validated in accordance with the most recent international standard. information from the ansm states that the french recall is being undertaken because of regulatory non-compliance. they have further stated that they have not identified a health risk associated with this issue. in australia, the tga has suspended further supply of these implants until it has finalized its investigation and determined that the implants are safe for use. tga has sought information from ansm and from the french manufacturer so that a decision about further supply of these implants can be made. for details, please refer to the following link:http://www.Tga.Gov.Au/safety/alerts-device-cereform-breast-implants-140221.Htm if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 24 february 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Cereplas Cereform silicone gel-filled breast implants
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    DH