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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The Ansm has been informed of the implementation on June 15, 2012, of a batch recall of "Dialer XEVONTA Hi 20, B Braun Avitum". Reference: 720466. Lots: 140350412 and 14036041. The recipients concerned were informed directly by the laboratory and received the attached mail (22/06/2012) (29 KB).