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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Focus diagnostics has received some customer complaints of simplexa flu a/b & rsv lots with sporadic false positive rsv signals which may result in a higher rsv false positive rate. the potential false positive rsv results are unpredictable within the identified lots and may not be easily identified during testing. this issue is only seen with the rsv (m gene) fluorescent probe-primer. the influenza a/b results are not impacted since the fluorescent probe-primers to detect influenza a/b viruses are different than those detecting rsv.