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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Sale of unlicenced device in error. brought to the attention of radionics that 6 devices were involved three distal catheters are listed under device id 900335.
Model Catalog: DSC-M (Lot serial: ALL LOT NUMBERS); Model Catalog: DCS-H (Lot serial: ALL LOT NUMBERS); Model Catalog: DSC-L (Lot serial: ALL LOT NUMBERS); Model Catalog: XDC-2 (Lot serial: ALL LOT NUMBERS); Model Catalog: 13756 (Lot serial: ALL LOT NUMBERS); Model Catalog: 11331 (Lot serial: ALL LOT NUMBERS)