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 GA1205 lot of the reagent called Dimension® / Flex ™ Lipase Reagent Cartridge (LIP) - Ref.DF55A from DADE BEHRING SA is withdrawn from the market due to erroneous results with certain cartridges: lower values of the controls and patient samples.