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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Bd usa discovered that lot number 45602 of the bd procount progenitor cell enumeration kit (material no 340498) failed to meet internal stability specifications. failure of stability can result in poor resoluti.