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.
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Baxter corporation initiated an urgent product recall communication for certain lots of rapidfill syringe strip product code 90200 (order reference # h93890200) due to a sterility barrier breach. baxter has received complaints for breaches in the sterile packaging. corrective actions have been implemented. product shipped as of april 14 2014 is not affected by this action.