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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Liquid level detection errors occur when using gel tubes in the delfia xpress. with gel tubes the needle can be clotted when piercing the gel and clotted needles can increase the rate of liquid detection error.