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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Afssaps was informed on December 8th, 2006 of a recall of normal heat-up tubes level 1 DI-60HL carried out by the company Smiths Medical on November 20th, 2006 following cases of rise in temperature beyond the programmed temperature warming liquid. The health facilities concerned by the recall received the attached letter (08/12/2006) (134 KB).