Recall Or Safety Alert for Clinical Chemistry Analyzers AU2700 / AU2700 Plus and AU5400, (Customers with complete MOD (modifications) AU2700-184 and AU-5400-190), manufactured between April 1999 and July 2012

According to Agencia Española de Medicamentos y Productos Sanitarios (Via FOI), this recall or safety alert involved a device in Spain that was produced by N/A.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Recall / Safety Alert
  • Date
  • Event Country
  • Event Source
  • Event Source URL
  • Notes / Alerts
    The data from Spain is current through June 2018. All of the data comes from Agencia Española de Medicamentos y Productos Sanitarios, 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 Spain.
  • Extra notes in the data
  • Action
    Possibility that the connection of the tube / tank of the concentrated detergent tank of the Clinical Chemical Analyzers AU2700 / AU2700 Plus and AU 5400, with the complete modifications AU2700-184 and AU-5400-190, deteriorates and presents leaks.


  • Source