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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Cardinal health has determined the specimen pitchers (fg65-4357a the specimen pitcher graduated 1200 cc) contained in these presource kits may be brittle due to design changes. as a result of stacking the pitchers inside each other breakage of the small internal ribs of the pitcher may occur.