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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Ocd has received complaints from customers reporting that caps on several reagent red blood cell product vials are too tight. in some of those complaints customers reported breaking or cracking of the glass reagent vial while attempting to unscrew the cap prior to use.