Alerta De Seguridad O Notificaciones De Seguridad para Autopen 24 1 unit pen, Autopen 24 2 unit pen, Autopen Classic 1 unit pen, Autopen Classic 2 unit pen

Según Medicines and Healthcare products Regulatory Agency, este evento ( alerta de seguridad o notificaciones de seguridad ) involucró a un dispositivo médico en United Kingdom que fue producido por manufacturer #17429.

¿Qué es esto?

Las notificaciones de seguridad de campo son comunicaciones sobre acciones que se pueden estar tomando en relación con un producto que se encuentra en el mercado, enviadas por los fabricantes de dispositivos médicos o sus representantes. Estas notificaciones son principalmente para trabajadores de la salud, pero también para usuarios. Pueden incluir alertas y retiro de equipos.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    MDA/2014/047
  • Número del evento
    CON491138
  • Fecha
    2014-12-17
  • Fecha de publicación del evento
    2014-12-17
  • País del evento
  • Fuente del evento
    MHRA
  • URL de la fuente del evento
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 recall data from the U.S. and the United Kingdom.
  • Notas adicionales en la data
  • Causa
    Risk of hyperglycaemia, which could lead to immediate and long-term deterioration of health. affected devices may have a mechanical fault which could cause the dose selector to revert to zero resulting in the devices not delivering the correct dose of insulin.
  • Acción
    Advise users to stop using affected devices and to seek a replacement pen.  Ensure that a suitable alternative device is available to enable them to maintain their insulin regime. Discontinue supply of all affected devices. Quarantine and return any remaining stock of affected devices to the manufacturer. Pharmacists Healthcare professionals Those involved in purchasing, supplying and using these devices.

Device

  • Modelo / Serial
  • Descripción del producto
    Autopen 24 1 unit pen Product code: AN4210. PIP code 293-5096. Autopen 24 2 unit pen. Product code: AN4200. PIP code 293-5070. Autopen Classic 1 unit pen. Product code: AN3810. PIP code 273-3178. Autopen Classic 2 unit pen. Product code: AN3800. PIP code 260-3561. To identify affected devices still within their packaging, look for the following packaging lot codes on the outer carton. Packaging lot code Product code Product name 7VJ AN3810 3ml 1 Unit Autopen Classic 7WB AN4200 Autopen 24 3ml 2 Unit 7WC AN4210 Autopen 24 3ml 1 Unit 7WD AN3800 3ml 2 Unit Autopen Classic 8CN AN4200 Autopen 24 3ml 2 Unit 8CP AN4200 Autopen 24 3ml 2 Unit 8CR AN4210 Autopen 24 3ml 1 Unit 8EL AN3800 3ml 2 Unit Autopen Classic 8EM AN3810 3ml 1 Unit Autopen Classic 8JK AN4210 Autopen 24 3ml 1 Unit 8JM AN3800 3ml 2 Unit Autopen Classic 8JN AN3810 3ml 1 Unit Autopen Classic 8JP AN4210 Autopen 24 3ml 1 Unit 8VV AN4200 Autopen 24 3ml 2 Unit 8VW AN4200 Autopen 24 3ml 1 Unit To identify affected devices without packaging look for the following production lot codes, which can be found on the lower part of the pen body. Production lot code (stamped on pen) Product code Product name 7RT AN3810 3ml 1 Unit Autopen Classic 7PN AN4200 Autopen 24 3ml 2 Unit 7PP AN4210 Autopen 24 3ml 1 Unit 7RV AN3800 3ml 2 Unit Autopen Classic 8KK AN3800 3ml 2 Unit Autopen Classic 8XD AN4200 Autopen 24 3ml 2 Unit
  • Manufacturer

Manufacturer