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
Five (5) firmware problems have been identified with the operon surgical tables. the problems are with tables that contain firmware version 3.010 6.00 or 6.010. all the problems occur at extreme movement limits and do not present a risk to the patient or user.