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 an issue with the navious flow cytometer with version 1.0 software: red and violet laser related errors are not displayed in the event of a laser failure. the blue laser is not impacted by this issue.
Model Catalog: A52103 (Lot serial: SERIAL NUMBERS AM51001-AS15102); Model Catalog: A52102 (Lot serial: SERIAL NUMBERS AN06024-AS03008); Model Catalog: A52101 (Lot serial: SERIAL NUMBERS AN29103-AS15099)