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. was notified by their supplier synthes (usa) of six complaints reported outside the us associated with synex ii implant (central body) which fully or partially collapsed in situ after a period of six to fifteen months post operatively.
Model Catalog: 04.808.003 (Lot serial: ALL LOTS); Model Catalog: 04.808.004 (Lot serial: ALL LOTS); Model Catalog: 04.808.011 (Lot serial: ALL LOTS); Model Catalog: 04.808.006 (Lot serial: ALL LOTS); Model Catalog: 04.808.001 (Lot serial: ALL LOTS); Model Catalog: 04.808.002 (Lot serial: ALL LOTS); Model Catalog: 04.808.005 (Lot serial: ALL LOTS); Model Catalog: 04.808.010 (Lot serial: ALL LOTS); Model Catalog: 04.808.009 (Lot serial: ALL LOTS); Model Catalog: 04.808.008 (Lot serial: ALL LOTS); Model Catalog: 04.808.007 (Lot serial: ALL LOTS)