Alerta De Seguridad para uretero-reno videoscopes and uretero-reno fiberscopes

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

¿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
    2017-01-09
  • Fecha de publicación del evento
    2017-01-09
  • 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: olympus uretero-reno videoscopes and uretero-reno fiberscopes medical device manufacturer, olympus, has issued medical device safety alerts concerning its uretero-reno videoscopes (model numbers: urf-v2 and urf-v2r) and uretero-reno fiberscopes (model numbers: urf-p6 and uf- p6r). for uretero-reno videoscopes, the manufacturer has initiated a corrective action following investigation of customer complaints regarding the breakage of the urf-v2/v2r insertion tube bending section during surgical procedures. to date, some of these complaints are associated with tissue trauma (including one complaint of perforation, and two complaints of insertion tubes which were stuck inside the patient and had to be surgically removed). for uretero-reno fiberscopes, the manufacturer has received complaints on the urf-p6/p6r insertion tube, and breaks of the bending tube, but these complaints have not resulted in any known adverse events. the manufacturer is aware of adverse event complaints on the urf-v2/v2r endoscopes which have a similar structure to the urfp6/p6r endoscopes. the manufacturer advises customers to inspect their inventory for the referenced devices and follow the recommended inspection procedures listed in the “instruction for safe use”. 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 9 january 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Olympus Uretero-reno Videoscopes and Uretero-reno Fiberscopes
  • Manufacturer

Manufacturer