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
Capture-r ready indicator cells do not meet reagent specifications. see preliminary report.
Model Catalog: (Lot serial: pro.code 5042lot4317930kits); Model Catalog: (Lot serial: licence ID 001079); Model Catalog: (Lot serial: prod.code 5047lot4318112kits)