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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There is a potential issue when entering the clinitek atlas control lot information into the clinitek novus analyzer for the bottle lot numbers p0001105 p0003115 n0006115. this is due to a missing alpha character at the end of the lot number on the control bottles for example: lot p0001105 instead of p0001105x.