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 will commence a remediation strategy whereby all current colleague pump customers will be provided with a newly manufactured colleague p1.7a pump software version 8.01.90 (en) or 8.11.90 (fr) in exchange for each existing pump with an earlier software version. this remediation is being conducted to correct pump issues previously communicated on january 29 2009 (recall number 45280 baxter reference 2008fca18) and to provide other software and mechanical upgrades.