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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All batches of micro-connector needle electrodes reference 034AMB001 BIOMEDIS whose expiry is less than or equal to March 30, 2003 were withdrawn from the market following the validation of the sterilization .. Given the small number of recipients of these devices, these have been warned directly by the manufacturer. As a result, no alert number has been assigned to this withdrawal.