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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The guides have the potential to remove more bone than necessary resulting in an increased cement mantle when used in a cemented femoral component application.
Model Catalog: 8050-5103 (Lot serial: ALL LOTS); Model Catalog: 8050-5105 (Lot serial: ALL LOTS); Model Catalog: 8050-5107 (Lot serial: ALL LOTS); Model Catalog: 8050-5109 (Lot serial: ALL LOTS); Model Catalog: 8050-5111 (Lot serial: ALL LOTS); Model Catalog: 8050-5113 (Lot serial: ALL LOTS)