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 batches 49001M100, 51758M300 and 51585M300 of the reagent called "IMx ESTRADIOL" ref: 2215-22 of the ABBOTT FRANCE company are withdrawn from the market following a risk of lowered result for the samples whose estradiol level is higher than 1000 pg / ml.