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 nrbc differential or reticulocyte mix chamber drain ports may become plugged by rubber pieces from specimen tube caps and result in biohazard or chemical exposure and/or the potential for generating incorrect results.