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 low level of occurrence (<0.02%) of the lumen exit and lumen size on the extension line being misprinted on certain central venous catheters. as an example the distal lumen may be printed with the word 'medial 18 ga' instead of 'distal 16ga'. the misprint does not impact the use of the product including use of individual lumens for infusion blood draws etc. the color coding of all hubs is correct and corresponds to the arrow system" white = proximal lumen grey = medial lumen 1 blue = medial lumen 2 brown = distal lumen.