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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Specific lots of check valves used in several locations within the lh 750 and lh780 analyzers may fail. this failure may result in an air or liquid leak at the connection to the vacuum overflow tank waste line or at the backwash tank drain line.