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 6 December 2002, ALL-DIAG withdrew from the market STA 20202 (per 02/2004) the in vitro diagnostic medical device called STREPTOP A - reference 5443, following a stability problem on certain test strips that could lead to , after a storage period of five months, the appearance of false positive results. ALL-Diag directly informed the 107 laboratories of medical analyzes concerned by this batch of device used for the research of Streptococcus A.