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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Bard peripheral vascular (bpv) is recalling specific lots of bard conquest pta balloon dilatation catheter because of deflation-related issues. in the event a pta balloon will not deflate immediate intervention is required in order to deflate the balloon and allow for continued blood flow.