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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Boxes of 510-101 lot 53226 and 500-101 lot 53240 were packaged at the same time during final packaging. final packaging consists of placing sealed sterile pouched tubes in boxes and labeling the boxes. some of the final packed boxes had a mixture of these two tubes. all pouches were packaged and labeled correctly.