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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Nxstage has identified a software error in the nxstage system one s cycler model no. nx1000-3 with software versions 4.9 and 4.10. if specific conditions are met and a software error does occur the ultrafiltration (uf) volume target will not decrease during the treatment even if the uf pump is running.