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
Carl zeis callisto eye assistance with software version 3.0 or 3.1 material number 301640-3010-300. during our continuous internal testing we found a software error when switching between day and night mode. this error disables some of the assistant functions and could lead to poor refractive outcome.