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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Welding was not conducted appropriately at a couple of points of the caster holding frame. this problem relates to an inadequate mechanical condition at the holding frame caused by inadequate mfring process.