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 confirmed an error in the package inserts pertaining to ca++ and lactate control ranges for rapid qc complete controls. the level 3 ica++ falls low on the rp400 and the lactate level 1 on the rl 1200 is also a concern.