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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Based on field recovery data siemens healthcare diagnostics has confirmed that the ph parameter may recover low within range or lower than expected with these three lots of level 3 rapidqc complete product on both the rapidpoint and the rapidlab blood gas systems.