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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Devices shipped to accounts without appropriate csa approval.
Model Catalog: 2L3210 (Lot serial: BETWEEN NOV. 2001 & AUG. 2002.); Model Catalog: 2L3210 (Lot serial: ALL DEVICES DISTRIBUTED); Model Catalog: 2M8171 (Lot serial: BETWEEN NOV. 2001 & AUG. 2002.); Model Catalog: 2M8171 (Lot serial: ALL DEVICE DISTRIBUTED); Model Catalog: 2L3100 (Lot serial: BETWEEN NOV. 2001 & AUG. 2002); Model Catalog: 2L3100 (Lot serial: ALL DEVICES DISTRIBUTED); Model Catalog: 2L3216 (Lot serial: ALL DEVICES DISTRIBUTED); Model Catalog: 2L3216 (Lot serial: BETWEEN NOVEMBER 2001 &); Model Catalog: 2L3216 (Lot serial: AUGUST 2002.); Model Catalog: 1M8550 (Lot serial: BETWEEN NOVEMBER 2001 &); Model Catalog: 1M8550 (Lot serial: AUGUST 2002.); Model Catalog: 5M5509 (Lot serial: ALL DEVICES DISTRIBUTED); Model Catalog: 5M5509 (Lot serial: BETWEEN NOV. 2001 & AUG. 2002.); Model Catalog: 1M8550 (Lot serial: ALL DEVICES DISTRIBUTED); Model Catalog: 2M9832 (Lot serial: BETWEEN NOV. 2001 & AUG. 2002); Model Catalog: 2M9832 (Lot serial: ALL DEVICES DISTRIBUTED); Model Catalog: 2L3213 (Lot serial: AU