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 issuing a safety alert to dialysis center clinicians to make them aware of safeguards that should be considered with seizure prone patients and other at-risk patients unable to care for themselves due to transient or permanent impairments during homechoice peritoneal dialysis therapy. this follows a reported patient death linked to tubing entanglement around the neck.