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
Afssaps was informed on 15/12/10 of the implementation of a recall made by Teleflex. The directors, local correspondents of materiovigilance and pharmacists of the health establishments concerned have received the attached letter (31/12/2010) (36 KB).