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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Cryostat seriel 45847 may have been built using an incorrect cable with undersized diameter. it could potentially cause cable to overheat and to break. if instrument not grouned according to ifu a severe risk of electric shock may result.