Alerta De Seguridad para CAS I/II Absorbers installed in the BleaseSirius and BleaseFocus Anesthesia Workstations

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

¿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
    2013-11-28
  • Fecha de publicación del evento
    2013-11-28
  • 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: spacelabs healthcare cas i/ii absorbers installed in the bleasesirius and bleasefocus anesthesia workstations the united states food and drug administration (fda) has issued a medical device safety alert concerning the recall of cas i/ii absorbers installed in the bleasesirius and bleasefocus anesthesia workstations, manufactured by spacelabs healthcare. the affected products are identified as follows: part no.: 12200900, 12200901, 12200902, 12200903, 14200100 service kits part number: 050-0659-00 and 050-0901-00 manufacturing date: 21 feb 2013 through 30 sep 2013 due to a potential defect in the affected products, the bag to-vent switch in cas i/ii absorbers may fail due to loose fastening hardware in an absorber. in the worst case, this would result in a large leak from the absorber circuit while operating in bag mode and could impede the ability to provide ventilation in bag mode. operation in vent mode along with all monitoring and alarm functions will continue to operate normally. customers with questions were advised to contact spacelabs healthcare for technical support. for details, please visit the following fda websites: http://www.Fda.Gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ucm376772.Htm http://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm376764.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 28 november 2013.

Device

  • Modelo / Serial
  • Clasificación del producto
  • Descripción del producto
    Medical Device Safety Alert: Spacelabs Healthcare CAS I/II Absorbers installed in the BleaseSirius and BleaseFocus Anesthesia Workstations
  • Manufacturer

Manufacturer