Notificaciones De Seguridad De Campo acerca de CELL-DYN Emerald Cleaner

Según Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), este evento ( notificaciones de seguridad de campo ) involucró a un dispositivo médico en Slovenia que fue producido por Abbott Laboratories.

¿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
    Field Safety Notice
  • Fecha
  • País del evento
  • Fuente del evento
  • Notas / Alertas
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 Slovenia.
  • Notas adicionales en la data
  • Causa
    The purpose of this letter is to inform you of a product recall for cell-dyn emerald cleaner lots 7044, 7082, 7110, and 7119, and to provide you with instructions on what actions your laboratory must take. abbott previously identified occurrences where the cell-dyn emerald analyzer generates quality control (qc) out of range low for parameters rbc and plt when using emerald cleaner lots 6853, 6901, 6953, 6991, 7024 and 7027. testing of cleaner lots 7044, 7082, 7110 and 7119 confirmed rbc and plt controls out of range. cause for the qc material out- of-range low issue has been traced to the manufacturing process for a raw material used in the cell-dyn emerald cleaner. actions have been taken to help verify acceptable performance of replacement product. in the interim, immediate action is necessary. .


  • Modelo / Serial
    09H46-02 7044 31JAN2018 N/A 09H46-02 7082 28FEB2018 N/A 09H46-02 7110 31MAR2018 N/A 09H46-02 7119 30APR2018 N/A
  • Manufacturer


  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source