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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The Afssaps was informed on 12/03/2012 of the implementation of two batch recalls carried out on 21/10/2011 and 16/02/2012 by the company Le Maitre Vascular. The users concerned have received the enclosed letters (27/03/2012) (545 KB).