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 23/12/10 of the implementation of an extension of the recall of batches carried out by the company Micrus Endovascular in October 201.. The institutions concerned by this extension of recall have received the attached mail (30/12/2010) (226 KB).