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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There is a possibility that the wrong pump tube connector was used in the production of lot 09/11. the incorrect pump tube connector (tr-69 in place of tr-10) which is a closed connector was used. as the heparin line is assembled to this connector if the closed type is used the heparin line will be occluded.