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
In agreement with Afssaps, the company Meditec Zeiss, informed, on 19/10/09, users of certain surgical kits for ophthalmology, a batch recall. The users concerned, in France, received the attached mail (23/10/2009) (42 KB). This information is intended for managers of operating theaters, local correspondents of materiovigilance, pharmacists and directors of health establishments for dissemination to the services concerned.