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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A discrepant inoculum density range has been identified for the neisseria haemophilus (nh) identification (id) test card in the vitek 2 7.01 product information document (ref 514740-1xx1 where xx indicates the language translation code).
Model Catalog: 27530 (Lot serial: Not applicable); Model Catalog: 27225 (Lot serial: Not Applicable); Model Catalog: 27560 (Lot serial: Not Applicable)