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 corporation has issued an important product information communication to advise customers regarding changes that are being made to instructions for use (ifu) for various baxter pd (peritoneal dialysis) transfer set product codes. baxter is updating these ifus to improve product labeling and ensure consistency of information across the baxter transfer set product family. see also recall number 82893.