Alerta De Seguridad para Rusch Belly Bag Urine Collection Bag with Hip Belt

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

¿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
    2013-04-05
  • Fecha de publicación del evento
    2013-04-05
  • 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: teleflex rusch belly bag urine collection bag with hip belt the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning rusch belly bag urine collection bag with hip belt [model and part no.: belly bag 1000ml b1000, belly bag with 24inch drain b1000ct, belly bag with sample port b1000p], manufactured by teleflex medical. the manufacturer has issued a voluntary recall for the above products as the packaging may be compromised, and therefore the sterility of the product cannot be guaranteed. if non-sterile products are used, there is a possible risk of infection. the manufacturer requests that medical staff to check their inventory for product within the scope of this field action. they should cease use and distribution of the affected product; and to quarantine immediately and return the affected product to teleflex for replacement. they also advises distributor of the affected products to the field safety notice to all of their customers. for details, please visit the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/ fieldsafetynotices/con252005 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 5 april 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Teleflex Rusch Belly Bag Urine Collection Bag with Hip Belt
  • Manufacturer

Manufacturer