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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Lot 400-2 (per 30.10.00) of the reagent called Identification Panel - reference 86930 from the company BIO-RAD is withdrawn from the market due to an error in the phenotyping of erythrocytes in tubing no. These red blood cells are Kpa -, Lea - b - and not Kpa +, Lea - b +. There are no other Kpa + red cells in this lot.