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 is issuing a device correction for homechoice and homechoice pro devices shipped without the english (language) patient at-home guide kit. home peritoneal dialysis patients who received a device without the patient at-home guide kit are being contacted by telephone and will be immediately shipped the guide kit.