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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The above lot is failing to meet the inhibition specification for the quality control organism escherichia coli atcc 2592 i.E. 2 log inhibition. this lot however supports the growth of salmonella spp. to the required specification and not all e.Coli species are impacted and acceptable inhibition was observed with some strains.