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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The pooling software can create pools containing more or less donors than originally intended during simultaneous pooling runs for both the cobas taqscreen mpx and cobas taqscreen wnv tests when the donor tube carrier on the hamilton star/starlet pipettor is missing a donor tube in any position within the donor tube carrier.