Retiro De Equipo O Alerta De Seguridad para "SynchroMed® II" implantable drug infusion pumps, models 8637-20 and 8637-40, manufactured between December 5, 2014 and February 10, 2015, with certain serial numbers

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.