Alerta De Seguridad para Arterial Venous Fistula (AVF) sets for Haemodialysis - Safety AVF Needle fixed wing

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

¿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
    2015-11-26
  • Fecha de publicación del evento
    2015-11-26
  • 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: kawasumi laboratories inc. arterial venous fistula (avf) sets for haemodialysis - safety avf needle fixed wing the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning the arterial venous fistula (avf) sets for haemodialysis - safety avf needle fixed wing manufactured by kawasumi laboratories inc. the affected catalogue numbers are avfe1525clfg and avfe1525cplfg and the affected lot numbers include 140714i8, 141014i5, 141110i1, 150128i7, 150511i1, 140912i6, 141110i2. the manufacturer has received four reports worldwide where the needle cannula of the arterial venous fistula set for haemodialysis had separated from the needle hub and remained in the patient’s vein when attempting to remove the needle following the completion of the dialysis treatment. although the possibility of occurrence for such an event is extremely low, there is potential that blood leakage could occur should the needle cannula separate from the hub and remain in the patient’s vein. there have been no reports of patient injury as a result of this issue. the manufacturer advises users to stop using the affected products from the affected population. customers are advised to quarantine and destroy all affected products in the affected population. for details, please refer to the tga website: http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2015-rn-01147-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 26 november 2015.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Kawasumi Laboratories Inc. Arterial Venous Fistula (AVF) sets for Haemodialysis - Safety AVF Needle fixed wing
  • Manufacturer

Manufacturer