Alerta De Seguridad para EnVe® ventilator

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

¿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
    2012-07-19
  • Fecha de publicación del evento
    2012-07-19
  • 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: carefusion enve® ventilator the united states food and drug administration (fda) has posted a safety alert concerning enve® ventilator, manufactured between december 2010 and january 2012, by carefusion. the manufacturer had identified potential risks associated with the enve® ventilator.A leak may occur in the patient breathing circuit or the system, resulting in the ventilator not holding the set positive end expiratory pressure (peep) value either intermittently or continuously. the device will activate both audible and visual alarms to notify the health care professional that ventilation delivery to the patient may be compromised. to date, there have been no reports of patient harm associated with the affected devices. for details, please refer to the fda website http://www.Fda.Gov/safety/recalls/ucm312682.Htm. posted on 19 july 2012.

Device

  • Modelo / Serial
  • Clasificación del producto
  • Descripción del producto
    Medical Device Safety Alert: CareFusion EnVe® ventilator
  • Manufacturer

Manufacturer