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
A technical investigation has indicated that the above lot may not react strongly with all strains of listeria monocytogenes when used in the microbact listeria 12l kit (mb1128a) thus making interpretation of the result more difficult than with alternate batches. continued use of this batch may lead to negative reporting.