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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Under extreme conditions of vigorous shaking of the package or enough shock/kinetic energy apply to package in a certain way the product potentially can pierce the tyvek pouch. the product is gamma irradiated for sterilization purposes and puncturing of the tyvek pouch will compromise the sterility of the product.