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 user can reproduce a free-flow condition if the clinician does not close the roller clamp on the iv administration set prior to opening the pump door and the pump door is opened by using a "flick" of the door latch that causes the door to "pop" open instead of opening the door by slowly raising the latch. this flicking motion may cause the centered sear design to not effectively engage with the safety clamp fitment which can cause unintended flow possibly resulting in an over infusion to the patient.