Alerta De Seguridad para FemoSeal Vascular Closure Systems

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Terumo Medical 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
    2017-08-22
  • Fecha de publicación del evento
    2017-08-22
  • 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 femoseal vascular closure systems medical device manufacturer, terumo medical corporation, has issued a safety alert concerning its femoseal vascular closure systems [product reference code: c11202]. the manufacturer is initiating a voluntary recall of select production lots of femoseal vascular closure systems in response to an increase in device related malfunction complaints. specifically, after the deployment of the inner locking disc, complaints allege that the button will not spring back as intended, preventing the outer locking disc from deploying and completing the procedure. when this failure occurs, options for the clinician include manual compression or surgical cut down. upon further review, devices associated with this complaint mode (approximately 1/600 per current complaint date) reflect the internal entrapment of the device’s suture assembly. suture entrapment prevents the proper actuation of the device to complete the surgical procedure. internal controls have been established in manufacturing to eliminate the potential for this defect. product replacement is on-going. 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 22 august 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Terumo FemoSeal Vascular Closure Systems
  • Manufacturer

Manufacturer