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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Siemens medical solutions usa inc. was made aware by the supplier that a potentially defective component was used in the line connection box (lcb) for a limited number of production systems. the lcb breaker may trip unnecessarily during normal operating conditions. this field action will replace the affected component and increase the stability of the breaker.