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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Potential for flickering (intermittent break-up of the on-screen video image) in the video laryngoscopy image when glidescope titanium su laryngoscope blades are in use.
Model Catalog: 0574-0131 (Lot serial: lots 081114 to 090315); Model Catalog: 0574-0132 (Lot serial: lots 022514 to 101915); Model Catalog: 0574-0133 (Lot serial: lots 022514 to 101915); Model Catalog: 0574-0133 (Lot serial: lots 072314 to 101515); Model Catalog: 0574-0132 (Lot serial: lots 072314 to 101515); Model Catalog: 0574-0130 (Lot serial: lots 081814 to 103015); Model Catalog: 0574-0131 (Lot serial: lots 081814 to 103015); Model Catalog: 0574-0130 (Lot serial: lots 081114 to 090315)