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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Two complaints were received reporting the dc power cable (p/n 3010556) jacket attached to the veris unit melted. the root cause investigation determined a design reliability issue at one of the cable terminations was found to be a contributing factor since it allows the wires at the end of the cables to be bent and twisted during use which can lead to electrical shorting.