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
High number of pressure abort (e2008) errors observed in the field when using gxgbs-100n-10 lots 08006 08007 08008 08009 08010 08011 08012 08401 08402 08403 08404 08405 08406 08407 08408 08409 08410 09201 and 09202.