Alerta De Seguridad para Ventlab Resuscitator Bags

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

¿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
    2014-05-19
  • Fecha de publicación del evento
    2014-05-19
  • 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: ventlab resuscitator bags the united states food and drug administration (fda) has issued a medical device safety alert concerning ventlab resuscitator bags, manufactured from ventlab, llc. the manufacturer has initiated a voluntary medical device removal of a limited number of ventlab resuscitator bags after becoming aware of complaints regarding a sticking duckbill valve that resulted in the resuscitation bags delivering no air through the patient valve, to the patient. the valves may stick due to incomplete curing during the manufacturing process. resuscitation bags affected may not function properly and may result in a delay of treatment and life threatening health consequences that include hypoxia and hypoventilation. there has been one report of injury requiring medical intervention due to the lack of a functional resuscitation bag and 31 reports of a delay in oxygenation due to the requirement to utilize a 2nd or 3rd device. the manufacturer advises users to stop using the affected products and return these products to the manufacturer. for details, please refer to the fda websites: http://www.Fda.Gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ucm397749.Htm http://www.Fda.Gov/safety/recalls/ucm397682.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 19 may 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Ventlab Resuscitator Bags
  • Manufacturer

Manufacturer