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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Notification to customers that unlicenced medical devices were sold.
Model Catalog: E7187 (Lot serial: ALL LOT NUMBERS); Model Catalog: MVS1061L (Lot serial: ALL LOT NUMBERS); Model Catalog: ET4750 A23 (Lot serial: ALL LOT NUMBERS); Model Catalog: N8177 (Lot serial: ALL LOT NUMBERS.); Model Catalog: E3123 (Lot serial: ALL LOT NUMBERS); Model Catalog: N7550 (Lot serial: ALL LOT NUMBERS); Model Catalog: N2472 (Lot serial: ALL LOT NUMBERS); Model Catalog: N0610 (Lot serial: ALL LOT NUMBERS); Model Catalog: N2530 (Lot serial: ALL LOT NUMBERS); Model Catalog: N1698 57 (Lot serial: ALL LOT NUMBERS); Model Catalog: N5941 5A (Lot serial: ALL LOT NUMBERS); Model Catalog: N5941 4 (Lot serial: ALL LOT NUMBERS); Model Catalog: E0566S (Lot serial: ALL LOT NUMBERS); Model Catalog: E0566SA (Lot serial: ALL LOT NUMBERS); Model Catalog: 109-2725 (Lot serial: ALL LOT NUMBERS); Model Catalog: E0566 (Lot serial: ALL LOT NUMBERS); Model Catalog: SP7-55978 (Lot serial: ALL LOT NUMBERS); Model Catalog: E2488 (Lot serial: ALL LOT NUMBERS); Model Catalog: N1690 11J (Lot serial: ALL LOT NUMBERS); Mode