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 SIEMENS company has informed the users of the N Latex IgM reagent of the recall of three lots .. The users concerned, in France, have received the attached mail (03/02/2015) (218 ko). address to the directors of health establishments and local correspondents of reactovigilance for diffusion to the services concerned.