Alerta De Seguridad para Trade name: Infusion Pump. Technical Name: Infusion Pump. ANVISA registration number: 80113010024. Risk class: III. Model Affected: Infusion Pump GH / Infusion Pump PK. Serial numbers affected: pumps manufactured prior to September / 2008 - attached list.

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por Respiratory Care Hospitalar LTDA.; Carefusion Switzerland 317 Sarl..

¿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
  • ID del evento
    2408
  • Fecha
    2017-11-16
  • País del evento
  • Fuente del evento
    ANVISA
  • URL de la fuente del evento
  • Notas / Alertas
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • Notas adicionales en la data
    If a pl3 alarm occurs the syringe pump should be immediately withdrawn from clinical use and should be referred for repair by qualified service personnel or authorized technical assistance. Additional information: - Date of identification of the problem by the company: 06/11/2017 - Date of notification notice to Anvisa: 11/16/2017 The company that owns the affected product is responsible for contacting its customers in due time. to ensure the effectiveness of the Field Action in progress. It stands out the joint responsibility of the distribution chain and use of health products in maintaining its quality, safety and efficacy, as well as the effectiveness of the Field Action, expressed by RDC 23/2012: "(...) Art 2 ° A holder of registration of health product is the holder of the registration / registration of health product with Anvisa. Single paragraph. The registration holder, as well as other agents involved from the production to the use of the product, or discarding it when applicable, are jointly and severally responsible for maintaining the quality, safety and efficacy of the health products to the final consumer. Art. 12 Distributors of health products shall forward to the registration holder, in a timely manner, the distribution map and other information requested for the notification and execution of field actions. (...) "
  • Causa
    Error code pl3 is an alarm indicating that the equipment is malfunctioning. alarm pl3 causes the device to stop working and warns the user of an internal fault by sending an error message together with a light signal and a steady high alarm that can not be silenced.
  • Acción
    Field Action Code PL3-ALARM triggered under the responsibility of Respiratory Care Hospitalar LTDA. Will make the Notice to the client.

Manufacturer