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.
데이터 추가 비고
원인
Due to an implementation error in production 10 symphony instruments (s/n 390051 to 390060) were manufactured and distributed with software v1.3.2 installed with a v1.3.1 dual air safety valve configuration rather than the v1.3.2 single air safety valve configuration.