Alerta De Seguridad para Tubing set, dialysis/haemodialysis (4008 HD Bloodlines)

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Fresenius Medical Care AG & Co KGaA.

¿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
    2018-04-13
  • Fecha de publicación del evento
    2018-04-13
  • 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: fresenius medical care australia - tubing set, dialysis/haemodialysis (4008 hd bloodlines) therapeutic goods administration (tga), australia, has issued a medical device safety alert concerning 4008 hd bloodlines [av/fres 2008-4008 (f00007119) and av/fres 4008 (f00007120)], manufactured by fresenius medical care ag & co kgaa. the manufacturer has been made aware of incidents regarding quality, safety and performance of the 4008 hd bloodlines tubing. the currently supplied roller clamp may cause customers to experience difficulties in handling that might result in excessive force being used to close the clamp causing the roller part to detach. this may cause infusion of saline solution in the event of incorrect use of the roller clamp, if the second clamp present on the arterial line is also damaged or not closed. according to the manufacturer, a number of leakages were reported at several locations on the 4008 bloodline tubing systems. leakages on the bloodlines may cause blood loss into the environment and may lead to air intake into the system. while the air intake is normally detected by the dialysis machine’s air detector, a leakage of blood may not be detected. the affected users are advised to follow the instructions for use in each carton box of the hd bloodlines: ensure that all caps and connections are secure; inspect the extracorporeal circuit for leaks during priming phase and treatment, taking corrective measures (e.G. tightening luer-lock connection) or exchanging the bloodline as necessary; ensure that no excessive force is applied on the roller clamp on the reinfusion set in order to regulate the flow of fluid through the infusion pathway. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 13 april 2018.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Fresenius Medical Care Australia - Tubing set, dialysis/haemodialysis (4008 HD Bloodlines)
  • Manufacturer

Manufacturer