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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A small percentage of units shipped from august 2010 - november 2010 could have a crack on the bottom of the sample site which could result in a small amount of leakage of intravenous fluids or blood.