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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Afssaps was informed of a recall of bladder catheters Grasset AC6507 lot 03101443 made by the company PORGES March 19, 2004 following a non-compliance of the tensile strength. Health facilities concerned by the recall in France received the attached letter (19/04/2004) (116 KB). The other competent European authorities are not concerned by this recall.