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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Siemens has identified an issue when scanning the 2d barcode for the master curve card (mcc) with advia centaur systems t3 kit lots ending in 198 on the advia centaur xpt system. an un-recoverable error which requires a field service visit to restore operation may occur on the advia centaur xpt system when the mcc for advia centaur systems t3 kit lots ending in 198 is scanned on the system.