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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Manufacturer has received complaints reporting that reprocessed lf1637 or lf4318 ligasures experienced compatibility issues when connected to the ft10 generator. an "invalid instrument" error message may appear on ft10 generators with software revision 1.1.5.4 when devices without an rfid chip are connected to the generator. updates were made to the ifu to provide clarity on software compatibility.