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 Beckman Coulter withdraws from the market batches with a number equal to or less than 107727 of the in vitro diagnostic medical device called: ACCESS ESTRADIOL - reference 33540 following a reagent safety volume below the quality standards set by the manufacturer.