Retiro De Equipo O Alerta De Seguridad para ARCHITECT c4000 Cuvette Segment (cuvette segment), reference 02P75-01; ARCHITECT c8000 Cuvette Segment (segment cuvettes) reference 01G46-01; ARCHITECT c16000 Cuvette Segment (segment cuvettes), reference 09D32-05

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.