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 distributor Prodis informed the 10/03/2014, the users of the double spatulas of Seibel (references SPA30-224 A / P and SPA30-224 B / P) of the manufacturer PISCES EYE INSTRUMENTS of a recall of all the batches of these devices .. Users concerned in France have received the attached mail (18/03/2014) (149 KB) .. Additional investigations of the ANSM are currently underway.