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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A trima accel device demonstrated a nonrecoverable power failure. a subsequent investigation of the failure determined that a power filter cable a component used in the internal electrical system had a visible defect which caused the unit to lose power. further evaluation determined that this defect may be present in other electrical cables which could cause a similar non-recoverable power failure.