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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This lot of media was not manufactured to the specified formualtion which resulted in an incorrect ratio of bile salts being added. continued use may result in false negative reporting incorrect bacteria counts and/or incorrect bacteria identification.