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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Immucor has had complaints of hemolysis in wb corqc tube 1 of this kit lot. the investigation has demonstrated microbial contamination in one example of wb corqc tube 1. wb corqc tube 1 lot 232192 is a component of wb corqc kit lot 236154 and 236154a. the product expired on 2013-02-07.