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
During regular maintenance of the ultrasonic mixer cover (usm cover 3) of the cobas c501 and cobas c502 a potential injury could occur if the customer does not notice the clearly visible sharp edge while removing the screws.