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.
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Steris has identified the control board software in select amsco 400 units will interrupt and cancel a processing cycle should the selected sterilizer shutdown time coincide with a processing cycle. this may result in a procedure delay should the facility immediately require instruments from the cancelled processing cycle. if the processing cycle is interrupted the cycle should not be considered complete and the instruments should be reprocessed. steris has received no reports of procedure delays associated with the occurrence of these events.