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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In agreement with the ANSM, the URGO LABORATORIES proceed to a recall of product URGO VERRUES TENACES. The pharmacists concerned received the attached mail (03/08/2012) (17 KB). Read more. A press release giving more information to end users on this recall is also available. Recall of the anti-wart product "Urgo Stubborn Warts" - Press release