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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Hemocue became aware of a production related problem which has affected some of the packaging material for single packed hb201 microcuvettes. if a single pack pouch is damaged the microcuvette can be exposed to moisture which in some cases may lead to a cuvette not filling or air bubbles being formed.