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 error code displayed on the screen can lead to misinterpretation which could potentially delay the treatement of patient with very low blood glucose.
Model Catalog: 12216841001 (Lot serial: TOUS LES LOTS); Model Catalog: 12138999001 (Lot serial: TOUS LES LOTS); Model Catalog: 03330494001 (Lot serial: TOUS LES LOTS); Model Catalog: 03035123001 (Lot serial: ALL LOTS)