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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At the request of Afssaps, the company Ypsomed proceeded to recall batches of blood glucose meter strips mylife Pura. The people concerned received the following letters. mail users (17/02/2012) (3325 KB mail pharmacists (17/02/2012) (2576 KB) A press release giving more information on this recall is also available on the Afssaps website.