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 company MEDRAD withdraws from the market batches 29764, 29765 and 29766 sterile syringes CT Tri-Pak reference CTP-200-FLS which are used with the CT injectors following the risk of exceeding the maximum endotoxin level defined in their specifications.