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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Pk cmv-pa reactive and non-reactive control vials from affected lots may contain lint. presence of lint in the control tubes has the potential to interfere with photometry and the controls may not test as expected and necessitate the run be repeated. donor results are not impacted by this issue.