Alerta De Seguridad para THERMOCOOL SF NAV Diagnostic/Ablation Deflectable Tip Catheter

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

¿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
    2014-04-15
  • Fecha de publicación del evento
    2014-04-15
  • 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: biosense webstar thermocool sf nav diagnostic/ablation deflectable tip catheter the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning thermocool sf nav diagnostic/ablation deflectable tip catheter, manufactured by biosense webster. the manufacturer has identified a higher frequency of spontaneously reported adverse events related to cardiac perforations and atrio-esophageal fistula (aef) with the uni-directional and bi-directional thermocool sf nav catheter family during the time period of january 2010 to december 2013 as compared to other navigational thermocool ablation catheters. the manufacturer has not yet identified a definitive cause for this observed difference in frequency of adverse events for the uni-directional and bi-directional thermocool sf nav catheter family. meanwhile, the manufacturer advises that two factors should be considered in relation to these reported adverse events: the increased stiffness and the related handling properties of the thermocool sf nav catheter family may contribute to the risk for perforation. due to the enhanced cooling feature of the thermocool sf nav catheter, application of the same power settings, guided by temperature feedback, as previously used with other navigational thermocool catheters may result in relatively deeper lesions and potentially contributes to higher rate of aef and cardiac perforations. the manufacturer also reminds users to pay special attention on relevant warnings and precautions in the instructions for use (ifu) for the thermocoolsf nav catheter family models. according to the local supplier, johnson & johnson (hong kong) ltd, the affected products were distributed in hong kong. for details, please refer to the following link:http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con402544 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 15 april 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Biosense Webstar THERMOCOOL SF NAV Diagnostic/Ablation Deflectable Tip Catheter
  • Manufacturer

Manufacturer