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 diagnostic has observed an increase in the frequency of complaints for vessel feeder errors. the errors observed include "670: vessel feeder track sensor stuck on full" and "749: vessel track empty". complaints have been confirmed with several dimension reaction vessel lots. a low percentage of reaction vessels from those lots have been observed to have flashing on the flange of the vessel that may jam in the vessel track and generate an error.