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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Through the conmed linvatec complaint system we have documented complaints of low or no flow or difficulty to regulate flow for the insufflators. the substance build up on the filters was identified as hytrel used in hose manufacturing.