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
Bd has determined that a quantity of product packaged within experimental shelf cartons made of recycled cardboard was released to consumers within lot 0039920. each of the experimental shelf cartons is labeled with an orange "change control" sticker identifying it as the experimental material. note: only the outer packaging shelf carton material was "experimental". the actual syringe products and inner sterility barrier packaging were all the correct qualified materials .