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
Through customer feedback and field service experience steris has learned that amsco v-pro 1 and v-pro 1 plus low temperature sterilization systems users may experience premature wear of the vacuum pump and filtering components. users may also experience incomplete aeration of the device's chamber following a failed leak test.