Alerta De Seguridad para nMARQ Circular Irrigated 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
    2015-07-03
  • Fecha de publicación del evento
    2015-07-03
  • 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 nmarq circular irrigated catheter medical device manufacturer, biosense webster, has issued a medical device safety alert concerning nmarq circular irrigated catheter [catalogue number: d132214, lot number: all]. the manufacturer has recently received an increased number of complaints related to a low temperature measurement anomaly at electrodes of the nmarq circular irrigated catheter. during the same time period, they have also received three reports of deaths of patients who were treated with the nmarq circular irrigated catheter. two of these cases were confirmed to be caused by atrio-esophageal fistula (aef). extensive ablation on the left atrial posterior wall may have been the main contributing factor to the aefs in these two cases of persistent atrial fibrillation that were treated by pulmonary vein isolation and left atrial posterior wall ablation. according to the manufacturer, no direct link could be confirmed between the low temperature issue and the aef as it was detected in only one of the two confirmed aef cases. therefore, the low temperature issue may be a secondary risk factor as it may affect power titration and delivery during radio frequency ablation. the manufacturer decided to conduct a removal for all lots of the nmarq circular irrigated catheter distributed since 2 february 2015 and conduct a full investigation. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 3 july 2015.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Biosense Webster nMARQ Circular Irrigated Catheter
  • Manufacturer

Manufacturer