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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Asept InMed informed Afssaps on March 26, 2003, that it is recalling all batches of SYRINGE-SYRINGE FITTINGS, reference R01, manufactured by EMP. The enclosed mail (27/03/2003) (8 KB) was sent to the 70 user centers to warn them of the recall of these products, only marketed in France.