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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A technical investigation has indicated that the cartridges of this lot of oxoid antimicrobial susceptibility testind discs amp10 (ampicillin) may contain individual discs that are not impregnated with antibiotic. continued use of this lot could result in false indication of resistance to ampicillin.