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. received notification from its supplier that a medical device recall was being initiated for the holding forceps for synream reaming rod due to a nonconformance found during the transfer of the machining operation from one location to another. the identified nonconformance is for the locking lever that has an incorrect angle.