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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At the request of the Afssaps, the company EUROS withdraws from the market some batches of sterile implants (for hip, knee, shoulder) following high values of initial contamination before sterilization. Given the small number of recipients, the manufacturer has informed them directly by sending them the list of references and lots concerned. For any information, you can contact EUROS at 04 42 71 42 71.