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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Synthes (canada) ltd. received notification from its suppliersynthes usa that a medical device recall was initiated for 5.0mm staineless steel rods (various part numbers)due to manufacturing non-conformance.
Model Catalog: 298.278 (Lot serial: all lots); Model Catalog: 298.277 (Lot serial: all lots); Model Catalog: 298.276 (Lot serial: all lots); Model Catalog: 298.275 (Lot serial: all lots); Model Catalog: 298.269 (Lot serial: all lots); Model Catalog: 298.273 (Lot serial: all lots); Model Catalog: 298.272 (Lot serial: all lots); Model Catalog: 298.271 (Lot serial: all lots); Model Catalog: 298.270 (Lot serial: all lots); Model Catalog: 298.274 (Lot serial: all lots)