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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Reports of fractured journey partial tibial knee baseplate components have been received. if a breakage/fracture occurs the broken baseplate must be revised and/or changed. if left unrevised a broken base could lead to instability and premature wear of the construct.