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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Mislabelled primary carton. the carton identified a portion of affected lots as 9546hp though the product was actually 9536hp as indicated on the pouch and the shipper. the udi code printed on the carton correctly identified the 9536hp product.