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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The recall is to inform affected customers of a possible interference between the t-handle on the hraim and the crw arc system and rework affected hraim devices by providing a new design hrimtsc t handle screw.