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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Vascutek has recently identified that a labeling error has occurred during packaging for graft catalogue # 733020. it has been incorrectly labeled as graft # 732030. # 733020 relates to 30cm usable length and 20mm internal diameter while # 732030 relates to 20cm usable length and 30mm internal diameter.