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
On january 25 2010 carestream health received a customer complaint indicating that the customer had opened a box of film and although it was supposed to be t-mat l/ra it was performing like t-mat g/ra.