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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On january 11 2011 baxter corporation notified customers that energizer c-size alkaline batteries should not be used with the infus.O.R. pump (recall number 60650). the purpose of this new communication is to inform customers that: a second device the mini-infuser system uses the same size battery and incorporates the same battery contact interface and that other brands of c-size alkaline batteries may incorporate the same feature that inhibits electrical contact.