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
Stryker has become aware during an investigation that the drill (combo reamer drill) is not able to perforate the bone substitute plate and it was not possible to drill a hole in bovine bone after manufacturing testing. therefore the acceptance criteria were not met.