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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Biosite inc. initiates voluntary recall for the triage drugs of abuse panel biosite catalogue number 95000 lot# 186625. the pcp (phencyclidine) test results in the panel kit gives false positives. discontinue all use of lot #186625 and discard affected product in accordance with local regulations.