Alerta De Seguridad para Prismaflex Control Unit

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Baxter 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
    2018-05-07
  • Fecha de publicación del evento
    2018-05-07
  • 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: baxter healthcare prismaflex control unit medical device manufacturer, baxter healthcare, has issued a medical device safety alert concerning its prismaflex control unit, details product models and serial numbers as below: product: 1) prismaflex 4.11; 2) prismaflex 5.00 row; 3) prismaflex 6.10 row; 4) prismaflex 7.11; 5) prismaflex 7.Xx row; 6) prismaflex system serial number: all the manufacturer will be installing new firmware on all prismaflex control units to address for the units to exhibit a failure mode with the pump module electronics. the failure mode may result in a “voltage out of range” malfunction alarm, which causes the device to enter a “safe state” and become inoperable until it is serviced. according to the manufacturer, the “voltage out of range” malfunction alarm causes the prismaflex control unit to enter a “safe state” by stopping all pumps and closing the return line clamp. this failure mode can occur at any time during use and may result in an interruption and/or delay in therapy. patient harm is not expected as the blood may be manually return to the patient. according to the local supplier, there were no associated adverse events, patient injury and product complaints reported in hong kong. the manufacturer advises that operators may continue to safely use prismaflex control units that have not exhibited the “voltage out of range” malfunction alarm. the manufacturer will be releasing new firmware that will prevent the malfunction from occurring. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 7 may 2018.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Baxter Healthcare Prismaflex Control Unit
  • Manufacturer

Manufacturer