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
Erratum to mail sent on 27/02 / 2013ANSM has been informed of the implementation of a recall made by Perouse Plastie. The health professionals concerned have received the enclosed letter which cancels and replaces (08/03/2013) (367 ko the mail sent on 27/02/2013 (details of the lots concerned).