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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In response to complaints that homechoice devices are excessively noisy baxter is updating the homechoice patient at-home guide to include a discussion of the expected operating sounds during therapy. customers are advised that if there is a significant change in the sound level or a new previously unheard sound when using the homechoice cycler please contact your doctor and/or nurse or baxter technical services.