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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In agreement with the AFSSAPS, the company CONTROLE GRAPHIQUE, following several incidents of materiovigilance, decided to proceed to the withdrawal of the plates concerned and sent the attached mail (12/06/2002) (6 KB), informing of this measure the directors and correspondents of materiovigilance of the establishments concerned.