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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While the pump is infusing a breakage of the plunger backplate spring may allow movement of the syringe plunger that may result in siphonage. neonatal and paediatric patients or those receiving critical drugs at low infusion rates would be considered to be the most at risk if small volumes of fluids reach the patient due to siphoning.