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
Defective component in the connector of the administration set. a male luer exhibits a sink condition which is the result of insufficient holding pressure during the injection mold process. the possibility of a leak increases when the male luer is used with a shorter female luer connector.