Alerta De Seguridad para Life Pulse High-Frequency Ventilator Patient Circuits

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

¿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
    2012-12-06
  • Fecha de publicación del evento
    2012-12-06
  • 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: bunnell life pulse high-frequency ventilator patient circuits the united states food and drug administration (fda) posted a firm press release concerning life pulse high-frequency ventilator patient circuits, manufactured by bunnell incorporated. bunnell incorporated voluntarily initiated a nationwide recall notification of life pulse high-frequency ventilator patient circuits. the product has been found to have heater wire insulation that can melt, causing sparking and smoke close to the humidifier cartridge. there have been 12 reported failures out of 5,771 patient circuits distributed. although there have been no reports of patient injury or death the manufacturer informs clinicians to be aware of the potential that a patient circuit failure could result in patient injury or death as a precautionary measure. for details, please refer to the following fda website: http://www.Fda.Gov/safety/recalls/ucm330842.Htm. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 6 december 2012.

Device

Manufacturer