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 batches 731 406 301, 726 440 901, 736 137 701, 728 682 901, 737 692 801 of the reagent called ASL SLIDEX-ref 7234, from the company BIOMERIEUX SA, are withdrawn from the market because of a decrease in sensitivity that can lead to the absence of agglutination of certain samples (false negatives possible).