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 possibility that the seals may be creased which may potentially affect seal integrity. this defect is not likely to cause adverse health consequences as the adaptors are used as part of a non-sterile system.