Alerta De Seguridad para IntelliSpace Critical Care & Anesthesia Clinical Information System

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
    2014-11-28
  • Fecha de publicación del evento
    2014-11-28
  • 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: philips healthcare intellispace critical care & anesthesia clinical information system medical device manufacturer, philips healthcare, has issued a medical device safety alert concerning its intellispace critical care & anesthesia clinical information system. the affected devices are identified as follows:- 865047 intellivue clinical information portfolio (icip), rev d 865209 intellivue clinical information portfolio (icip), rev e 866072 intellispace critical care & anesthesia (icca), rev. f 866148 intellispace critical care & anesthesia (icca), rev. g according to the manufacturer, a software configuration defect has been identified that impacts one standard content (configuration that is shipped with the product) unit of measure (gm/m2). the defect involves an incorrect multiplier in the configuration that causes an incorrect calculation of medication dosage. the error could result in a calculated dose that is 10 times the correct dose. if the user does not identify that an incorrect multiplier exists in the standard content, a patient may receive a dose of medication that is incorrect (10 times the intended dosage). users are advised to implement the instructions outlined in the mandatory field change order (fco) if the body surface area (bsa) (gm/m2) standard content is used in the configuration. the manufacturer has initiated a correction to address this issue and a manufacturer’s representative will contact users to schedule the implementation of this correction. 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 28 november 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Philips Healthcare IntelliSpace Critical Care & Anesthesia Clinical Information System
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    DH