Alerta De Seguridad para Carestation 620, Carestation 650, and Carestation 650c Anaesthesia Systems

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por GE 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
    2017-10-13
  • Fecha de publicación del evento
    2017-10-13
  • 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: ge healthcare carestation 620, carestation 650, and carestation 650c anaesthesia systems the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning carestation 620, carestation 650, and carestation 650c anaesthesia systems, manufactured by ge healthcare. the manufacturer has recently become aware that an incomplete seal can exist between the co2 absorber and the breathing circuit co2 bypass port assembly of the carestation 600 series systems. an incomplete seal can allow rebreathing of patient gases that have bypassed the co2 absorbent material and could result in unintended elevated levels of inspired co2 (fico2), which could lead to hypercarbia. to date, there have been no injuries reported as a result of this issue. the manufacturer is advising users as an interim solution to increase the flow of fresh gas to reduce the volume of patient gas that is rebreathes if elevated fico2 levels are observed. if the fico2 levels cannot be adequately reduced with this action, users should consider switching to another anaesthesia delivery device. the manufacturer is releasing revised parts that minimise the likelihood of incomplete gas flow through the co2 absorbent canister. for details, please refer to the tga website: http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2017-rn-01300-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 13 october 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: GE Healthcare Carestation 620, Carestation 650, and Carestation 650c Anaesthesia Systems
  • Manufacturer

Manufacturer