Events

Alerta De Seguridad para Gemini, Precedence and Brilliance

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

¿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
    2012-07-11
  • Fecha de publicación del evento
    2012-07-11
  • País del evento
    Hong Kong
  • Fuente del evento
    DH
  • URL de la fuente del evento
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20120711.html
  • 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: philips gemini, precedence and brilliance medical device manufacturer, philips healthcare issued a medical device safety alert to remind philips gemini, precedence and brilliance users of the importance of careful reviewing and monitoring protocol parameters, especially when using the drop-down feature for mas/slice. philips also recommended the affected users to: review and carefully monitor each protocol selected before scanning the patient, the dose indices, specifically mas/slice, displayed on the control panel; make sure that the values displayed reasonably correspond to the doses normally associated with the protocol; always review and verify the mas/slice value before initiating any scan to prevent unintended radiation. based on the information provided by the local supplier, the affected products have been distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 11 july 2012.

Device

Gemini, Precedence and Brilliance
  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Philips Gemini, Precedence and Brilliance
  • Manufacturer
    Philips Healthcare

Manufacturer

Philips Healthcare
  • Empresa matriz del fabricante (2017)
    Philips
  • Source
    DH