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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Les tubulures du lot 07m15751 pourraient avoir ete assemblees avec la mauvaise ligne arterielle et le clamp arteriel pourrait ne pas etre assez fort pour permettre l'occlusion de a ligne.