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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Follows recall number 59046 (beckman coulter update letter dated april 20 2011 pca-14994). two additional lots of lh series pak reagent kits were not identified in the last communication. excess r flags and incomplete or abnormal differential computation results with use of coulter 5c cell control abnormal ii may also be encountered with lh series pak reagent kits lots 110882k and 110883k.