Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
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One lot of erytype s rh donor plates contains an error in the labelling on the foil packet. the product is correctly identified however the product description immediately below is incorrectly stated. the outer box information is correct as well as the barcode information on the plate frames and microplate strips.