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 manufacturer bio-rad medical diagnostics gmbh has recently notified us regarding a correction to the labeling provided with this product. donor cell i10 identified as donor number 550054 on the worksheet has been wrongly identified as leb (le2) positive. latest research could not confirm this determination.