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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Potential problem if servicing device and interchanging tubing between valve block level regulation and diaphragm pump if the functionality of the level regulation system is not tested as requested in the service manual. an interchanged tubing results in an inverse function of the manual level regulation system.