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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Certain compact absorbers used only with the ge healthcare adu anesthesia systems may have an increased resistance to gas flow due to an improperly manufactured foam filter.
Model Catalog: 427002100 (Lot serial: 133086-136086); Model Catalog: 427002000 (Lot serial: 133086-136086); Model Catalog: 427002100 (Lot serial: LOTS ENDING WITH 076 AND PRIOR); Model Catalog: 427002000 (Lot serial: LOTS ENDING WITH 076 AND PRIOR)