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
The amplification kit ce has a reagent registration button that contains incorrect expiration dating information. as a result after scanning the registration button information into the ventana instrument the kit will only provide a useful life through 19-july-2011. this incorrect date was entered in error and should have been 27-dec-2011.