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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Batches ATOC15 and ATOC25 (per.30.06.01) of the reagent called Syva rapid test THC - reference 6A029 - from the company DADE BEHRING SA are withdrawn from the market following the obtaining of false positive results for certain samples of patients having a concentration THC () 9-tetrahydrocannabinol) below the threshold level.