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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Baxter is recalling two (2) lots of vented spike adapter product code 2c0471 because of potential tears in the product pouches. a tear in the packaging can cause a breach in the sterile barrier.