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 is notifying cusyomers that the instructions for use (ifu) included with the named bardex i.C. 2-way foley catheters and 2-way council tip foley catheters distributed by the manufacturer from june 2013 to june 2015 provide the incorrect inflation volume. the inflation volume provided on the catheter's valve cap does state the correct inflation volume.