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 possible software bug of the accu-check inform ii meters with software versions 03.02.01 or 03.03.00 when configured to allow the operators to add new patient ids.
Model Catalog: 05060303001 (Lot serial: SOFTWARE VERSIONS); Model Catalog: 05060303001 (Lot serial: 03.03.01 AND 03.03.00); Model Catalog: 05060311001 (Lot serial: SOFTWARE VERSIONS); Model Catalog: 05060311001 (Lot serial: 03.03.01 AND 03.03.00)