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The lots 002000, 003000, 004000 of the reagent called SAFETY-TEST ABO / reference 79059 of the company DIAGAST are withdrawn from the market following the presence of PTU-AB card / reference 79054, batch 032000 among their constituents; this batch 032000 having been withdrawn on December 7, 2000.