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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ANSM has been informed of the implementation of a lot withdrawal carried out by SIEMENS. The affected users received the attached mail (14/10/2016) (169 KB). This safety action is registered with the ANSM under the number R1609590.