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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This field safety notice serves to notify customers that lane 42 (a24-34d) in the affected a high resolution ssp unitrays does not amplify a*2432 allele. this issue would produce a mistyping for a*2432 positive sample.