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) has confirmed that specific product code / lot number combinations may have an incorrectly sized blunt tip stylet within its packaging that will not pass through the coaxial. specifically the product should contain a 19 gauge blunt tip stylet when the actual packaged product contains a 17 gauge blunt tip stylet.