Alerta De Seguridad para Reusable Breathing Circuit

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Fisher and Paykel Healthcare 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
    2013-01-08
  • Fecha de publicación del evento
    2013-01-08
  • 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: fisher and paykel reusable breathing circuit the united states food and drug administration has issued a medical device safety alert concerning reusable breathing circuit [model no.: 900mr068 & lot no.: 110810 & 111020], manufactured by fisher and paykel healthcare ltd. according to the manufacturer, the tubes used in the reusable breathing circuit have pinholes. if these pinholes are not detected during the standard leak test before patient use, it could potentially result in a gas leak in the breathing system, which may lead to a loss of pressure for the intended ventilation therapy. usage of the defective device may result in patient death. customers were instructed to examine their inventory and destroy and discard any affected circuits in possession. replacement circuits will be provided to customers. according to the local supplier, the affected products were not distributed in hong kong. for further details, please refer to the fda websites: http://www.Fda.Gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ ucm334446.Htm http://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm334297.Htm if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 08 january 2013.

Device

Manufacturer