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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A rf suppression ferrite has to be added to the ethernet cable to consistently reduce emissions below the allowed limit for the stellant d dual syringe injector with certegra workstation causing a misbranding of the product.
Model Catalog: SCT-310 (Lot serial: SN 10493 10478 10473); Model Catalog: SCT-310 (Lot serial: SN 11295 10962 10516); Model Catalog: SCT-310 (Lot serial: SN 10409 10430 11036); Model Catalog: SCT-310 (Lot serial: SN 11047)