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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An anomaly was detected in the bact/alert 3d b.40.Xx firmware affecting bact/alert 3d signature and seleclink configuration. in specific circumstances the optimal growth detection algorithm may not be assigned to a bottle under test.