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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Typographical error on the vial labels. catalogue number (ref) and lot number (lot) symbols are switched. the labeling on the outer box and all other labeling accompanying the product is accurate. the reversed ref/lot symbols were noticed during in-house use of fdp02-10 lot d2-34 on nov.29 2017.