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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Inadequate secural may result if the tape is not firmly stroked or pressed onto both the skin and the tubing during application and could cause inadequate securing of tubes like endotrachial tubes.