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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Specific product codes and lot numbers of the endo femoral aimers may have been improperly marked indicating the wrong size and part number. the actual 4mm aimer is marked as 6mm and the actual 6mm aimer is marked as 4mm.
Model Catalog: 72201716 (Lot serial: For product code 72201714:); Model Catalog: 72201714 (Lot serial: For product code 72201714:); Model Catalog: 72201716 (Lot serial: (L)502780141 and (L)50278014); Model Catalog: 72201714 (Lot serial: (L)502780141 and (L)50278014); Model Catalog: 72201716 (Lot serial: For product code 72201716:); Model Catalog: 72201714 (Lot serial: For product code 72201716:); Model Catalog: 72201716 (Lot serial: (L) 50278012); Model Catalog: 72201714 (Lot serial: (L) 50278012)