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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Potential adverse events that may occur as a result of catheter tip fracture and or separation may include loss of device function medical intervention to retrieve a separated segment or complications resulting from a separated tip occluding blood flow to end organs.