Alerta De Seguridad para TF Adaptive Gutta Percha Point Size SM3-50pk

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Ormco 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
    2016-02-18
  • Fecha de publicación del evento
    2016-02-18
  • 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: ormco corporation tf adaptive gutta percha point size sm3-50pk medical device manufacturer, ormco corporation, has issued a medical device safety alert concerning its tf adaptive gutta percha point size sm3-50pk. [part number: 815-1541; lot number: ge15011637]. the manufacturer has become aware of a mismatch of the above product’s inner and outer labels. the outer package of the product is identified as sm3, which matches the product inside. however, the inner generic label is identified as ml3. according to the manufacturer, this product would be used correctly in a properly obturated canal. if a doctor removed the cover of the tray and is only looking at the inner label, he could mistakenly use the sm gutta percha with a ml file system. this sm3 gp will not properly fill the canal due to smaller size and can result in the gutta percha slipping past the apex of the root. product recall is on-going. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 18 february 2016.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Ormco Corporation TF Adaptive Gutta Percha Point Size SM3-50pk
  • Manufacturer

Manufacturer