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 Guidant company informed Afssaps on April 1, 2003 of a reminder it made on March 31, 2003 concerning Multi-Link Vision coronary stents with diameters from 2.75 mm to 4 mm. Guidant sent the attached mail (01/04/2003) (11 KB) on March 31 to the 73 user health facilities.