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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Microport orthopedics inc. removed part numbers 38025060 38025662 and 38025664 from an approved canadian license in november 2014. no product performance activity occurred for the resurfacing indication related to removal of these parts from the license. in december 2017 microport orthopedics inc. was made aware that the products were sold into canada after the november 2014 date of product removal from the license.