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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On August 20, 2002, Oxoid removed from the market batches 6794 (per 09.02.03), 7154 (per 09.02.03), 7537 (per 11.05.03), 7538 (per 09.02.03) and 7677 (per 06.03.03) of the in vitro diagnostic medical device known as Now Legionella - reference FR59091, following the possibility of obtaining false positive results.