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 endoscopy has become aware that the stryker heated insufflators may have been received with no expiration date printed on the label. additionally it was discovered that no packaging shelf-life testing had been completed for those products during the initial product launch. stryker has also become aware that the above referenced products may have been released for distribution and sold in countries that may have regulations regarding label expiration.