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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Perouse Medical has informed users of the chest tube of a product withdrawal. The users concerned, in France, received the attached mail (10/10/2012) (111 KB). This information is addressed to the directors of health establishments and local correspondents of materiovigilance for diffusion to the concerned services.