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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Smiths medical international ltd. has become aware that certain portex uncuffed paediatric tracheal tubes were manufactured with an internal diameter slightly smaller than specifications. there is a remote potential for a suction catheter to become lodged in a tracheal tube which may require extubation.
Model Catalog: 100/127/035 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100/127/030 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100/127/025 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100-134-030 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100/112/035 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100/112/030 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100-134-035 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100-141-035 (Lot serial: ALL LOTS MAY 2007-NOV 2008); Model Catalog: 100-141-025 (Lot serial: ALL LOTS MAY 2007-NOV 2008); Model Catalog: 100-141-030 (Lot serial: ALL LOTS MAY 2007-NOV 2008); Model Catalog: 100-105-030 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100-105-035 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100-105-025 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100-111-035 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalog: 100-111-030 (Lot serial: ALL LOTS PRIOR SEPT 2009); Model Catalo