Alerta De Seguridad para Misago Peripheral Self-Expanding Stent System

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

¿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
    2016-08-12
  • Fecha de publicación del evento
    2016-08-12
  • 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: terumo misago peripheral self-expanding stent system medical device manufacturer, terumo corporation, has issued a medical device safety alert concerning its misago peripheral self-expanding stent system. the affected devices are identified as follows:- product codes: all misago products starting with sf*f or sx-v lot number: all products on the market within the labeled expiration period (manufactured from september-2013 through august-2016) during the inspection process, the manufacturer identified a low occurrence rate of two types of non-conformances in comparison to the specifications as described in the regulatory applications: reduced diameter at one, or both ends of the stent due to incomplete self-expansion after release from the delivery catheter; and deformation of the stent strut shape due to the compression forces that are applied to compact, and mount the stent to the delivery catheter. according to the manufacturer, the body of clinical evidence as related to misago stents supports that clinical performance is not affected in that there are no new or additional complications, or adverse health consequences. the health hazard evaluation concluded that the nonconformity in the dimension (reduced diameter rat the ends of the stent), or in the stent shape (a bend or inconsistent alignment of the stent struts), will have no impact to safety, or effectiveness, of the product. therefore, there is no additional risk of serious health harm posed by these nonconforming products. the manufacturer has not received customer complaints, or adverse events, related to incomplete stent expansion, stent deployment failure, insufficient diameter, or stent deformation. product recall is ongoing. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 12 august 2016.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Terumo Misago Peripheral Self-Expanding Stent System
  • Manufacturer

Manufacturer