French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 France.
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Afssaps was informed on 02/09/10 of the implementation of a product recall carried out by Swissimplant. Users of this device had already received the enclosed letters. (09/09/2010) (2660 KB) Read more Solysafe septal occluder - Swissimplant - Safety information (26/10/2010)