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
If the pbs supply container is removed after instrument initialization and then reconnected to the fluidics module without any pbs in the container assays will continue to run without pbs. also if the waste container is removed after initialization and then reconnected to the fluidics module full of fluid assays will continue to run with a full waste container which could cause the container to overflow.