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 partial grid-switch failure may occur that may result in a higher xray dose than expected. the potential failure can lead to a radiation exposure rate in excess of 11.5/min (as required).
Model Catalog: 722016 (Lot serial: ); Model Catalog: ALLURA XPER FD20 (Lot serial: ); Model Catalog: ALLURA XPER FD10 (Lot serial: ); Model Catalog: ALLURA XPER FD20/10 (Lot serial: ); Model Catalog: ALLURA XPER FD10/10 (Lot serial: ); Model Catalog: 722043* (Lot serial: )