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 sidearm tubing may detach from the sheath during use. if this failure occures it may result in excessive patient blood loss and/or risk of blood-borne pathogen exposure to those in the surrounding area.