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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Letter and fax back form sent to all accounts describing the problem and instructions on obtaining overlays for the keypads.
Model Catalog: 2M8151 (Lot serial: ALL SERIAL #S PURCHASED OR); Model Catalog: 2M8163 (Lot serial: ALL SERIAL NUMBERS PURCHASED); Model Catalog: 2M8163 (Lot serial: OR LEASED FROM FEB. 2002 TO); Model Catalog: 2M8153 (Lot serial: OR LEASED FROM FEB. 2002 TO); Model Catalog: 2M8163 (Lot serial: APRIL 12 2004.); Model Catalog: 2M8153 (Lot serial: APRIL 12 2004.); Model Catalog: 2M8153 (Lot serial: ALL SERIAL NUMBERS PURCHASED); Model Catalog: 2M8161 (Lot serial: ALL SERIAL #S PURCHASED OR); Model Catalog: 2M8161 (Lot serial: 12 2004.); Model Catalog: 2M8151 (Lot serial: 12 2004.); Model Catalog: 2M8161 (Lot serial: LEASED FROM FE. 2002 TO APRIL); Model Catalog: 2M8151 (Lot serial: LEASED FROM FE. 2002 TO APRIL)