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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Stryker sustainability solutions has received an increase in reports indicating that an eeprom chip error code may occur when reprocessed 2515 nav eco variable electrophysiology (ep) catheters are used with carto? ep navigation systems. there have been no injuries reported as a result of this event.