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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The expiration dates listed on the iq body fluid controls - level i and level ii package labeling (vial assay sheet and kit box) do not correspond to the expiration date displayed by the iq200 analyzer.
Model Catalog: 800-3219 (Lot serial: KIT LOT 7030); Model Catalog: 800-3219 (Lot serial: KIT LOT 6340); Model Catalog: 800-3219 (Lot serial: KIT LOT 7086)