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 is releasing a performance update (xp050/15/p) to fix intermittent errors during tomo reconstruction with objects larger than 90mm on the mammomat inspiration system. the problem occurs because of a software bug in the memory mamangement of the graphics card memory. siemens field service reps will install new software version vb30p to correct the issue.