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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A drawing of the abutment retrieval instr zr cc rp/wp incorrectly defined the dimension of the functional length of the shell. this resulted in the product not working as intended for the removal of the rp and wp metal adapter.