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 has identified a specific set of system serial numbers that may have been manufactured with a card guide that has an extra lock washer.The extra washer is not necessary when assembling the card guide and may lead to damage of the electronic chassis components. if one of these components fails the system will become inoperable and stop sample processing.