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 batch OE146R (péremption15 / 05/2001) of the reagent called disks of CEFTAZIDIME 30mcg (code 66308) of the company BIO-RAD is withdrawn from the market, some cartridges of the batch containing 50 disks not impregnated with ceftazidime (risk of rendering results of false resistance to ceftazidime).