Alerta De Seguridad para THERMOCOOL SMARTTOUCH 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
    2014-10-23
  • Fecha de publicación del evento
    2014-10-23
  • 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 thermocool smarttouch catheter medical device manufacturer, biosense webster, has issued a medical device safety alert concerning its thermocool smarttouch catheter family [catalogue number: d132701, d132702, d132703, d132704, d132705, d133601, d133602, d133603; lot number: all]. biosense webster, a division of johnson & johnson medical nv/sa has observed 34 complaints with a frequency of 0.03% related to a bend/crack at different locations of the shaft of the thermocoolsmarttouch catheter during the time period of january 2012 to july 2014. none of the reported complaints were associated with any adverse events. through the investigation, manual pre-shaping of the distal shaft of the catheter and use of 8 fr sheaths were identified as the two primary causes of these events. the manufacturer would like to reinforce the following statements from the warnings and precautions and directions for use in the instructions for use (ifu) for the thermocool smarttouch catheter family: warnings and precautions: do not use excessive force to advance or withdraw the catheter when resistance is encountered. directions for use: to verify compatibility between the sheath and catheter, advance the catheter through the sheath prior to insertion. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 23 october 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Biosense Webster THERMOCOOL SMARTTOUCH Catheter
  • Manufacturer

Manufacturer