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
It has been determined that the expiration date indicated on the angiojet ultra thrombectomy system is beyond the original shlef life date. the safe use of the products throughout their currently labeled expiration dates the product is request to be returned.