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 received customer complaints regarding advia centaur xp version 6.0 systems that will experience an event that will require a reboot when a verification reagent used in manufacturing expires. the event will occur when event messages 700 00 01 and 700 00 02 are displayed.