Alerta De Seguridad para EXCOR® arterial cannula with graft CGRG-021

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

¿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
    2012-08-07
  • Fecha de publicación del evento
    2012-08-07
  • 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: berlin heart excor® arterial cannula with graft cgrg-021 the medicines and healthcare products regulatory agency (mhra), united kingdom (uk) posted a field safety notice concerning excor® arterial cannula with graft cgrg-021 manufactured by berlin heart gmbh. during the period from october 2011 to july 2012, the excor® arterial cannula with graft cgrg-021 (6 mm graft arterial cannula) was subject to a limited market launch with product monitoring. while evaluating the clinical data, berlin heart received an increasing number of cases in which, according to customer feedback, seroma and bleeding in the region of the graft material occurred. an analysis of the cause is in process. there is the risk that for patients who are provided with the excor® arterial cannula with graft cgrg-021 could experience seroma and bleeding, and as a result may require re-operation with a cannula exchange in individual case. on the basis of this information, berlin heart has decided to recall the excor® arterial cannula with graft cgrg-021 from the market. all other arterial cannulae from the product range continue to be available without limitation and can be used for implantations. for details, please refer to the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/index.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 7 august 2012.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Berlin Heart EXCOR® arterial cannula with graft CGRG-021
  • Manufacturer

Manufacturer