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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Based on scientific publications (including eucast warning letter on their website) on colistin gradient and disk diffusion tests including etest colistin biomerieux was alerted about a potential underestimation of the mic values for entero bacteriaceae and acinetobacter biomerieux initiated a complaint investigation to confirm product performance and determine root cause. while the internal and external investigations are still ongoing.