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.
데이터 추가 비고
조치
The ANSM has been informed of the implementation of a safety action / withdrawal of batch / withdrawal of product carried out by the company NIDACON INERNATIONAL AB. The users concerned received the attached mail (23/12/2015) (416 KB). This safety action is registered at ANSM under the number 201516750. You will be able to check its status on the Directory of Materiovigilance Reports by entering this registration number.