Alerta De Seguridad para Various Presource Kits Containing a Pre-Assembled Anesthesia Circuit

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

¿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
    2013-05-08
  • Fecha de publicación del evento
    2013-05-08
  • 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: cardinal health various presource kits containing a pre-assembled anesthesia circuit the united states food and drug administration (fda) has issued a medical device safety alert, concerning various presource kits containing a pre-assembled anesthesia circuit, manufactured by cardinal health. cardinal health discovered that various presource kits containing a pre-assembled anesthesia circuit and filter may contain outer plastic packaging on one or more components. if the packaging is removed without dissembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction in airflow. this may result in serious adverse health consequences including low blood oxygen (hypoxia), suffocation and death. according to the fda, cardinal health has notified customers of the problem and products affected on 26 march 2013 and advised customers to examine their inventories, identify and locate the products affected, notify clinicians, and affix a warning label on the front of each kit. the warning label instructs clinicians to remove and discard the anesthesia circuit and filter assembly. for details, please visit the following fda websites: http://www.Fda.Gov/safety/medwatch/safetyinformation/safety alertsforhumanmedicalproducts/ucm351024.Htm http://www.Fda.Gov/medicaldevices/safety/listofrecalls/ ucm350996.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 08 may 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Cardinal Health Various Presource Kits Containing a Pre-Assembled Anesthesia Circuit
  • Manufacturer

Manufacturer