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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Software v8.00.02 contains an anomaly that may cause a "sharp watchdog timeout" error message when a message is being written to the pump's event history log and the length of that message exactly matches the size of the available memory at the end of a memory sector. the software anomaly may result in a delay or interruption in therapy while an alternative pump is obtained.