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 company Becton Dickinson withdraws lot 29459 ProCOUNT kit (Progenitor Cell Enumeration Kit) - reference 340498, following a stability problem resulting in a decrease in the fluorescence intensity of the kit CD45 PerCP reagent.