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 the vented needle (305213) was incorrectly labeled at the unit package level with the non vented needle (305216) top web at the web at the unit packaging level. case carton and shelf carton were labeled properly with vented needle (305213) information.