Alerta De Seguridad para Medfusion Syringe Pump Model Series 3500 and 4000

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

¿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
    2017-08-02
  • Fecha de publicación del evento
    2017-08-02
  • 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: smiths medical medfusion syringe pump model series 3500 and 4000 the medicines and healthcare products regulatory agency (mhra) of the united kingdom has posted a medical device safety alert concerning medfusion syringe pump model series 3500 and 4000, manufactured by smiths medical. the manufacturer became aware that the thread lock material used on a fastening screw can be ineffective. as a result, the medfusion pump syringe barrel clamp mechanism may loosen and decrease the pump’s ability to accurately detect the outside diameter measurement of the syringe barrel, causing an “invalid syringe size” alarm to occur. a delay in the initiation of an infusion or an interruption of an active infusion has the potential to result in serious injury or death. the effect to the patient would depend on the patient’s condition, the therapy involved, and the amount of time the therapy would be delayed or interrupted. the “invalid syringe size” alarm triggered as a result of this potential issue alerts healthcare practitioners to the problem. although no serious injuries or deaths have been reported as a result of this issue, the manufacturer recommends against using the affected devices until repair work is completed. the users are instructed to locate the affected devices, which would be repaired by the manufacturer. for details, please refer to the mhra’s website: https://www.Gov.Uk/drug-device-alerts/field-safety-notice-24-to-28-july-2017 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 2 august 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Smiths Medical Medfusion Syringe Pump Model Series 3500 and 4000
  • Manufacturer

Manufacturer