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 corporation has issued a recall for the listed devices due to an increase in rupture complaints in product manufactured between november 2008 through january 2011. baxter has since implemented product and process improvements which have improved quality and reduced complaint rates for rupture. baxter wants to ensure that no affected product remains in the field.