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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Arthrocare corporation has determined that several lots of the saber 30 with integrated cable wands are subject to excessive movement in its plastic tray during shipping. the wands are not secured in the plastic tray and the movement can potentially render the product non-sterile in cases where the tip of the wand wears a small puncture or hole in the tyvek lid.