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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Potential issue with imprecise touch screen response for the meters which could lead to incorrect data entry. this issue would only occur in the manual patient id entry screen or in the date and time entry after a meter reset. if this issue occurs a patient id mismatch could take place.