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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Steris has learned that some customers may experience premature bulb failures due to loosening of wires and overheating of the lamp housing assemblies within the harmony la lc 500 and la 700 surgical lighting and media systems.