Retiro De Equipo O Alerta De Seguridad para Coronary endoprosthetic systems with drug release "BioMatrix Flex ™ and BioMatrix NeoFlex ™

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.