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.
데이터 추가 비고
조치
In agreement with Afssaps, the BARD company, informed October 31, 2008, the users of the WIZARD replacement balloon gastrostomy buttons of the recall of several batches (06/11/2008) (28 ko) of these products, following cases abroad, rupture leading to skin irritation. The users concerned, in France, have received the attached mail (06/11/2008) (16 KB). The competent European authorities have been informed of this measure by the manufacturer. This information is addressed to the directors of health establishments and local correspondents of materiovigilance for diffusion to the concerned services.