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 company ORGENTEC informed the users of the reagent Captia VZV IgM of the recall of a lot .. The users concerned, in France, received the email attached (29/04/2014) (40 ko) .. This information s address to the directors of health establishments and local correspondents of reactovigilance for diffusion to the services concerned.