Alerta De Seguridad para Carto® 3 Systems

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
    2012-02-21
  • 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
    Field safety notice: biosense webster carto® 3 systems the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning cartor 3 systems manufactured by biosense webster, inc. the manufacturer has recently become aware that some carto® 3 systems may be susceptible to ablation radio frequency interference through certain interconnected cable configurations. according to the manufacturer, the root cause has been determined to be a newly introduced patient interface unit (piu) backplane card. the new card is more sensitive to radio frequency interference, which will manifest as a jumping/ disappearing icon and/or error messages 105 and 319. biosense webster explained that while ablation at an unintended location could potentially happen as the result of undetected or ignored icon jumps, the likelihood of this happening is remote as the high detectability of icon jumps and the verification of catheter tip position with fluoro and/or ecg by operating physicians. as a result, the probability of a potential patient injury from icon jumps is unlikely and continued use of the carto® 3 systems remains safe and effective. biosense webster is going to replace the piu backplane card for the affected customers. meanwhile, customers are suggested to eliminate the radio frequency interference by utilizing the accessories provided with the customer notification. the notification also suggests ways to deal with the error messages. 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 product, please contact your supplier for necessary actions.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Biosense Webster Carto® 3 Systems
  • Manufacturer

Manufacturer