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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Batch No. 505492 of the reagent called: THROMBOREL S-code OUHP435, from the company DADE BEHRING is withdrawn from the market, following an extension of the Quick Time (exploration of the extrinsic pathway of coagulation) with some vials.