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 has been informed of the implementation of a recall of lots of disposable imaging accessories - COVIDIEN fittings and syringes distributed by the GUERBET and BAYER laboratories. The concerned recipients were informed by the GUERBET laboratory for the products provided by the latter (07/03/2012) (364 ko) and the BAYER customers were warned directly by COVIDIEN (07/03/2012) (107 KB)