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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Work lists containing reagent volumes greater than or equal to the specimen volume may cause instrument to omit the probe-wash step thereby contaminating daughter tubes and reagent vials hence erroneous results.