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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The ANSM has been informed of the implementation of recalls carried out by Gynéas. The users concerned have received the enclosed letters (19/01/2015) (280 KB). Read auss. Decision of 13 January 2015: suspension of the placing on the market, of import, distribution and use and withdrawal of medical devices manufactured by EUROBAND, a reprocessor of POLLAK, placed on the market after 1 June 2013