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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There is a labeling discrepancy specific to listed lot numbers of bardport titanium implanted port (pc 0602290). the end flap label indicates a different product description as compared to the main label. the main label identifies the port as a "titanium implanted port" while the end flap identifies the port as a "titanium low-profile implanted port". the product inside the kit is a regular port and not a low-profile port.