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 manufacturer has identified that the accu-chek inform ii + rf meters (cat # 05060303001 with serial numbers between uu14000000 and uu14100000) may have issues with poor touch screen response which could lead to incorrect data entry.