Alerta De Seguridad para Arrow Edge Hemodialysis Catherization Set Long-Term Access, Arrow NextStep Antegrade Hemodialysis Catheterization Set, Long-Term Access

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

¿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
    2014-02-11
  • Fecha de publicación del evento
    2014-02-11
  • 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: arrow international arrow edge hemodialysis catherization set long-term access, arrow nextstep antegrade hemodialysis catheterization set, long-term access the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning arrow edge hemodialysis catherization set long-term access, and arrow nextstep antegrade hemodialysis catheterization set, long-term access hemodialysis catheters, manufactured by arrow international, inc. the manufacturer has issued a voluntary recall for some lots of the hemodialysis catheter product codes due to receipt of complaints that the tunneling sheath packaged within the kits can crack during placement. if the tunneling sheath cracks, it can cause a delay in treatment for the time it takes to retrieve a replacement kit. the manufacturer advises users to cease use and distribution of stock of affected product and quarantine immediately. according to the local supplier, cemma enterprise, the devices were not distributed in hong kong. for details, please refer to the following link:http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con371783 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 11 february 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Arrow International Arrow Edge Hemodialysis Catherization Set Long-Term Access, Arrow NextStep Antegrade Hemodialysis Catheterization Set, Long-Term Access
  • Manufacturer

Manufacturer