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 Afssaps, the company Didactic, informed the users, on the 26/01/09, the recall of umbilical clamps of Bar. The users concerned, in France, received the attached mail (27/01/2009) (20 KB). This information is addressed to the directors of health establishments, local correspondents of materiovigilance and pharmacists for diffusion to the concerned services.