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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Baxter corporation has issued a device correction notice for a limited number of colleague single channel cxe pumps french p1.7a that were released but were found to have been tested to an incorrect voltage during the the dielectric voltage withstand test (hipot test) as part of the manufacturing process.