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
Baxter is issuing a product recall for all unexpired lots of 50mm 0.2 micron filter attachment product code 35 (order code h93835) due to the potential for the filter membrane layer to be missing and for particulate matter to be present in the fluid path. the affected lots were distributed between november 19 2013 and june 17 2016.