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.
데이터 추가 비고
원인
1-increase frequency of white screen alarm code 2-potential unrestricted flow when set is removed from the pump. moreover the check flow stop alarm intended to warn users of free flow conditions may not consistently operate as intended and may not reliably provide appropriate warning. 3-reports of symbiq pump not detecting air in line.