Alerta De Seguridad para Trade name: Products in sterile condition manufactured in the period from 03/03/2013 to 01/10/2017. Technical Name: N / A. ANVISA registration number: N / A. Risk class: III. Model Affected: N / A. Serial number affected: All lots supplied in sterile condition (gamma radiation) manufactured in the period from 03/03/2013 to 01/10/2017.

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por MDT Industria Comércio Importação e Exportação de Implantes S.A..

¿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
  • ID del evento
  • Fecha
  • País del evento
  • Fuente del evento
  • URL de la fuente del evento
  • Notas / Alertas
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • Notas adicionales en la data
    Always refer to the product's external label to verify that the product is within its shelf life and follow the directions in the instruction on using the product. If you wish to notify technical complaints and adverse events use the following channels: Notivisa: Notices of adverse events (AE) and technical complaints (QT) for products subject to Sanitary Surveillance should be made through the NOTIVISA System. To access the System, you must register and select the Health Professional option, if you are a liberal professional or the Institution / Entity option, if you are a professional of an institution / entity. Technovigilance System: Patient or citizen can notify through the Technovigilance System / SISTEC access through the link Additional information: - Date of identification of the problem by the company: 02/23/2018 - Date of notification notice to Anvisa: 05/03/2018 The company that owns the affected product is responsible for contacting its customers in due time. to ensure the effectiveness of the Field Action in progress. It stands out the joint responsibility of the distribution chain and use of health products in maintaining its quality, safety and efficacy, as well as the effectiveness of the Field Action, expressed by RDC 23/2012: "(...) Art 2 ° A holder of registration of health product is the holder of the registration / registration of health product with Anvisa. Single paragraph. The registration holder, as well as other agents involved from the production to the use of the product, or discarding it when applicable, are jointly and severally responsible for maintaining the quality, safety and efficacy of the health products to the final consumer. Art. 12 Distributors of health products shall forward to the registration holder, in a timely manner, the distribution map and other information requested for the notification and execution of field actions. (...) "
  • Causa
    Possibility of changing the hue of the chemical indicator to yellow-orange during storage of the products supplied in the sterile condition, however, we note that such a variation of hue is not associated with the shelf-life of the product and does not affect the safety and efficacy of the product. note: gamma radiation sterilization chemical indicator is used only for internal process controls and should not be used as a reference by the user to determine the sterility of the product.
  • Acción
    Field Action Code AC.2018.001 triggered under the responsibility of the company MDT Industria Comércio Importacao e Exportação de Implantes SA It will update or complement the instructions for use.