Alerta De Seguridad para CARTOSOUND Module of the CARTO 3 EP Navigation System

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
    2015-10-02
  • Fecha de publicación del evento
    2015-10-02
  • 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 webster cartosound module of the carto 3 ep navigation system medical device manufacturer, biosense webster, has issued a medical device safety alert concerning its cartosound module of the carto 3 ep navigation system, [catalogue number: c3sound] when used with the soundstar eco 8f and eco 10f diagnostic ultrasound catheter, [catalogue number: 10439236, 10439072, 10439011 & 10438577]. the manufacturer has received one complaint of image disappearance from the cardiac ultrasound system when the carto 3 ep navigation system needed restarting. this occurred while the patient was experiencing pericardial effusion. based on medical evaluation of the health risk profile, the manufacturer believes that the likelihood of harm to the patient is generally low if the ultrasound imaging is not available. however, if the intra-cardiac ultrasound is used to actively monitor an ongoing effusion, the lack of imaging may present a safety issue due to the delay in procuring the resources/equipment to use another imaging modality. the manufacturer will be updating the product labeling to include and further reinforce the above-mentioned precautionary safety information. according to the local supplier, the affected product [cartosound module for the cartro 3 ep navigation system] is distributed to hospitals in hong kong for demonstration purposes. however, soundstar eco 8f and eco 10f catheter are not distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 2 october 2015.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Biosense Webster CARTOSOUND Module of the CARTO 3 EP Navigation System
  • Manufacturer

Manufacturer