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 confirmed that there is a potential measurement error when using the auto-stats (auto statistics) measurement tool on acuson s family ultrasound systems with software versions vc25d vc30a and vc30b. the potential risk to the patient is the measurement and/or calculations will be incorrect and will have to be repeated.