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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Smiths medical has become aware of an increased trend in reports of disconnections of the luer lock connector at the patient end of the tubing on certain sets. if the luer lock connector disconnects during use this could result in fluid/ blood loss and/ or a delay in therapy which could result in patient injury or while highly unlikely death.