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
Software update to address 1) unexpected shutdown and device restart of the touchscreen resulting in settings returning to those stored in the clinic configuration of the device and loss of manual settings and 2) the possibility that electromagnetic interference due to electric current fluctuations may cause pressure values on the display to freeze.