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
Teleflex medical has issued recall due to the possibility that the nebulizer adaptor packaging may have open or weak seals which may affect the sterility of the adaptor. the adaptor product is labeled as sterile.