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 was informed by Applied Medical on 30/08/2012 of the dissemination of a corrective action concerning vascular catheters A44XX, A47XX, A4FXX and IRR-XXX-XX. The affected users have received the attached mail (11/09/2012) (404 KB).