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 recall has been initiated due to a labelling issue. cardinal health has received one report of customer receiving 65652-124 in a packaged labelled as 65652-123 with lot number 1091745 manufactured 11/16/2009.