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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Siemens healthcare diagnostics has determined that dimension vista loci thyroid stimulating hormone (tsh) lot 14237aa may produce falsely depressed results ranging from -23% to -96% near the end of the well set due to inadequate reagent volume in a flex well. the occurrence of this issue is low. quality control will detect the issue if it is run near the end of an affected well set.