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
There are typographical errors in the ifu number z870 which may cause hazardous situations if reprocessing is performed accordingly. this was discovered due to a reported complaint which occurred in the eu with no patient injury nor death reported.