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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During documentation review for three new vitek 2 ast gp test cards it was discovered that there is a cefoxitin screen (oxsf01n) "test by alternative method" limitation for staphylococcus pseudintermedius that is incorrect in or missing from various package inserts.