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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Animas ir 1200 insulin pumps that have sustained an external impact may have damaged the force sensor which can cause the whole cartridge of insulin to be dispensed during the "load cartridge" step of the priming sequence. failure to follow safety instructions and disconnect the infusion set from the body during the "rewind load and prime" steps can lead to unintended delivery of insulin.