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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The unicel dxh 800 coulter cellular analysis system with revision 2.0.0.1 system will not read codabar barcode labels at the primary reader under the following conditions: - the leading and trailing characters do not match (e.G. a12345b) - the aim-16 checksum digit calculation is used with any leading and trailing characters that are not both "a.".