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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Earlier this year the fda initiated an industry-wide action asking all companies that sell bone cement to include warnings about the potential for cardiac embolism in their ifus. this update was not initiated by any specific incident. all us companies that make/sell bone cement were asked to update their ifus.