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
Haemophilus test medium (htm) mp0806 lot 2220891 may not provide acceptable microbiological performance over time. although the product passed initial qc repeat qc testing has revealed a decrease in recovery of haemophilus influenzae atcc: 49766 10211 and 49247.