Alerta De Seguridad para Anaconda ONE- LOK Bifurcate Body and Anaconda Bifurcate Body

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

¿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
    2013-10-22
  • Fecha de publicación del evento
    2013-10-22
  • 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: terumo anaconda one- lok bifurcate body and anaconda bifurcate body medical device manufacturer, vascutek ltd, a terumo company, has issued a field safety notice concerning anaconda one-lok bifurcate body and anaconda bifurcate body. the affected catalogue numbers are as follows: anaconda one-lok bifurcate body: olb21, olb23, olb25, olb28, olb30, olb32, olb34 anaconda bifurcate body: b19, b21, b23, b25, b28, b30, b32, b34 vascutek ltd has received three complaints (with an occurrence rate of 0.1%) where the release wire of an anaconda body delivery system has fractured following stent deployment. two of these three incidents resulted in conversion to open repair. the voluntary recall addresses potential risks associated with the wire fracturing and the possibility of conversion to open repair. according to the manufacturer, this is a potential failure mode of to delivery system and does not affect the safety or efficacy of the implantable stent. previously implanted stents are not affected by this voluntary recall. furthermore, according to the manufacturer, there is no suggestion that patients already implanted with anaconda one- lok bifurcate body or anaconda bifuracte body are exposted to any raised level of risk. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 22 october 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Terumo Anaconda ONE- LOK Bifurcate Body and Anaconda Bifurcate Body
  • Manufacturer

Manufacturer