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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Beckman coulter has confirmed that the shuttle to barcode reader and cap piercer alignment procedure cannot be performed on dxc pro systems when the cap piercer is disabled. there is no impact if the cap piercer is not disabled and operating properly.