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 032000 (per 31.12.2000) of the reagent called card PTU AB - reference 79054 (ultimate pre-transfusion control card) of the company DIAGAST is withdrawn from the market following the possibility of observing, for some cards, a color change and, optionally, a change in reactivity of the dried antibodies.