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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Risk of tubing detaching from the oxygen mask connector either prior to use or during use disrupting oxygen supply to patient.
Model Catalog: 9108-E (Lot serial: > than 10 contact MFR); Model Catalog: 9106-E (Lot serial: > than 10 contact MFR); Model Catalog: 3266-E (Lot serial: > than 10 contact MFR); Model Catalog: 3226-E (Lot serial: > than 10 contact MFR); Model Catalog: 3106-E (Lot serial: > than 10 contact MFR); Model Catalog: 9226-E (Lot serial: > than 10 contact MFR); Model Catalog: 108-E (Lot serial: > than 10 contact MFR); Model Catalog: 106-E (Lot serial: > than 10 contact MFR); Model Catalog: 104-E (Lot serial: > than 10 contact MFR); Model Catalog: 3108-E (Lot serial: > than 10 contact MFR); Model Catalog: 3104-E (Lot serial: > than 10 contact MFR)