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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Some corometrics 174 series products were shipped incorrectly identifying the power cord as cf type for the fetal ecg function. although there is no iec standard requiring that fetal ecg parts be cf type a new power adaptor will solve this problem by making the product compliant to the cf type labeling on the product.