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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During inspection of incoming components from a supplier 3m discovered a valve with incorrectly labeled "input" and "output" orientation. identified in a single lot of 100 valves this defect can result in the valve being installed backwards creating a remote possibility of valve failure. because one of the uses for these valves is to admit air into the sterilizer chamber and also prevent eo (ethylene oxide) from escaping a failure may result in eo being vented outside the sealed chamber during a limited period (<1 minute) during the eo injection phase of the cycle.