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 has been informed of the implementation of the recall of a consignment of EUROBAG ® LOT GR 07807 urine bags. The recipients concerned have been informed directly by the laboratory and have received the enclosed letter (14/03 / 2012) (1341 KB).