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.
데이터 추가 비고
원인
The citrate (cit) and malonic acid (mlo) substrates are switched from their specified locations on the prongs of the crystal enteric lid. two customers have complained that they obtain a "no id" or "tie id" result when testing salmonella isolates. a third customer complained that the substrate reactions for cit and mlo were the opposite of what is expected for the known salmonella species they were testing.