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 that customers running the magnesium rtu assay on the abx pentra 400 chemistry analyzers that on-board stability has been updated. user will be unable to calibrate the magnesium rtu assay after 1 day of on-board (on instrument use) the control will be out of range at values lower than target values. the result reported using this failed calibration will be flagged "cal_error" displayed on the results with a "c".