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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Occasionally the specimen head will slowly advance on its own as if the advance knob is turned slightly forward. the issue has been identified as a small brass component notmeeting specified tolerances. only a small percentage of units identified by the serial number identified have this issue.