Notificaciones De Seguridad De Campo acerca de Check-Flo hemostasis assembly and others

Según Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), este evento ( notificaciones de seguridad de campo ) involucró a un dispositivo médico en Slovenia que fue producido por Cook Medical Europe.

¿Qué es esto?

Las notificaciones de seguridad de campo son comunicaciones sobre acciones que se pueden estar tomando en relación con un producto que se encuentra en el mercado, enviadas por los fabricantes de dispositivos médicos o sus representantes. Estas notificaciones son principalmente para trabajadores de la salud, pero también para usuarios. Pueden incluir alertas y retiro de equipos.

Más información acerca de la data acá
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2017-02-06
  • País del evento
  • Fuente del evento
    AMPMDRS
  • Notas / Alertas
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 recall data from the U.S. and Slovenia.
  • Notas adicionales en la data
  • Causa
    Cook medical begins the process of voluntarily recalling the above products and batch numbers. we have seen an increase in reports of blood loss related to devices whose design includes a special hemostatic valve (also called a "blue" valve or polyisoprene valve). in november 2015, products with blue haemostatic valves were either discontinued or replaced with products containing a different valve design with improved hemostasis. cook continued to receive reports of blood loss related to the previous generation of products with "blue" valves and therefore initiated the procedure described above in connection with these products.

Device

  • Modelo / Serial
    KCFN-4.0-18-13-RA-HC G35597 KCFN-4.0-18-23-RA-HC G35598 KCFN-4.0-18-7-RA-HC G35596 KCFN-5.0-18-13-RA-HC G35600 KCFN-5.0-18-13-RA-S-HC G35607 KCFN-5.0-18-23-RA-HC G35601 KCFN-5.0-18-7-RA-HC G35599 KCFN-6.0-18-13-RA-HC G35603 KCFN-6.0-18-13-RA-S-HC G35608 KCFN-6.0-18-23-RA-HC G35604 KCFN-6.0-18-23-RA-S-HC G35609 KCFN-6.0-18-7-RA-HC G35602 KCFN-7.0-18-13-RA-HC G35605 KCFN-7.0-18-23-RA-HC G35606 Komplet TriForce™ za periferni prehod KCXS-5.0-35-100-RB-0/0-HC G56416 KCXS-5.0-35-65-RB-0/0-HC G56412 KCXS-5.0-35-65-RB-0/DAV-HC G56413 KCXS-5.0-35-65-RB-MPB/DAV-HC G56415 Pripomoček za uvajanje Check- Flo ® Hausdorf-Lock atrijski RCFW-7.0-38-75-RB-HLA-091100- BV G03769 RCFW-8.0-38-75-RB-HLA-091100- BV G03770
  • Manufacturer

Manufacturer