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The CERIA company has withdrawn from the market on December 26th, 2006 the batches and the references specified in appendix, of the medical device called "femoral stems HELMED" following a case of postoperative rupture. The company has directly notified the recipients of the incriminated lots with the attached message (26/12/2006) (66 ko) validated by Afssaps. This information is intended for health facility directors and local correspondents for material vigilance for dissemination, where appropriate. appropriate to the services concerned. This reminder concerns only France.