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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An increased rate of initial reactive results was observed for specific lot of cobas mpx. as a consequence the manufacturer requests that customers discontinue and discard any remaining cobas mpx of lot number 238061.