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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Synthes (canada) ltd. is initiating a medical device recall for the drill bit due to the potential for the drill stop to slip on the reamer. if the drill stop slips on the reamer it may cause deeper reaming than intended and in rare cases penetration of the joint space causing pain and/or joint irritation.