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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ANSM has been informed of the implementation of a recall made by CERAVER. The affected users have received the attached mail. (27/02/2015) (223 KB) This security action is registered with the ANSM under the number 201501897 .. You will be able to consult its progress report on the Directory of the reports of materialovigilanc by entering this n ° of 'recording.