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
Product base pair size for a pcr amplicon was incorrectly labelled on product documentation. for the affected cw locus kits the product size for a primer mix was labelled as 110 base pairs where it should have been 200 base pairs. this problem does not cause a mistyping or a no typing but it may cause confusion within interpretation.