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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Stryker has received a report from the field of incorrect product information identified in trident surgical protocol lsp69 ("lsp69") and trident product reference guide lx3prg ("lx3prg"). lsp69 and lx3prg each contain the table which references an incorrect number of screw holes for trident hemispherical ha cluster shell sizes 44mm - 50mm.