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 STEDIM withdraws from the market lot 2/02822 of the medical device called "NUTRIPOCHE EVAM" reference FR103STD following the presence of a particle of cardboard in a pocket. This lot has been assigned to only one customer.