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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Use of the picc catheters that are subject to this recall may have an increased incidence of hemolyzed blood samples which may require additional peripheral access or replacement of the picc catheter. to date no patient injuries (mdrs) have been reported as a result of this issue.