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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Stryker has become aware that some of the hinge coupling packaging may contain incorrect product. this issue was first discovered via customer complaint november 17 2017 where it was reported that upon opening the 4933-0-800 [lot# 23745] it was discovered that the packaging contained product # 4933-1-011 [lot# 19865]. this pfa applies to all unopened/originally packaged product.