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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Afssaps was informed on 23/05/2011 of the implementation of a recall made by Stryker France. The affected users have received the attached mail (31/05/2011) (63 KB). Read auss. Unipolar head V40 for hip prosthesis - Stryker France - Security Information. (11/08/2011)