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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The reason for this recall/correction/removal is to inform dealers of defective product recently shipped to their facilities and to explain that when processed some sheets will show a pre-exposure fog. the removal request is to attempt to quarantine the affected material prior to it being shipped for customer use.