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: n ° 250499 and n ° 022699 of the reagent called: SECURICARD (references IJB 109010224 / IJB 109010124), of INSTITUT JACQUES BOY company are withdrawn from the market following a weakening of the anti-A antibody of this device of control pre-transfusional, leading to a possibility of misinterpretation of the test.