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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Future Medical Systems informed Afssaps on 03 October 2003 that it has recalled the FMS reference 4114 interfaces used in knee arthroscopy procedures. The company STRYKER, the only distributor in France of this device sent to the 21 establishments concerned on October 9, 2003 the attached mail (09/10/2003) (1253 ko).