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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An anomaly exists in the software which leads to a record save fail in the case that a partially treated fraction has zero dose accumulation. if the change to the plan had been to parameters other than dose per fraction treatment to incorrect volume could resultpotentially leading to serious injury.
Model Catalog: HIT (Lot serial: contact manufacturer.); Model Catalog: 8.6.07 (Lot serial: contact manufacturer.); Model Catalog: 8.5.11 (Lot serial: contact manufacturer.); Model Catalog: 8.1.15 (Lot serial: contact manufacturer.); Model Catalog: HIT (Lot serial: >10 serial numbers.); Model Catalog: 8.1.15 (Lot serial: >10 serial numbers.); Model Catalog: 8.6.07 (Lot serial: >10 serial numbers.); Model Catalog: 8.5.11 (Lot serial: >10 serial numbers.); Model Catalog: HIT (Lot serial: contact manufacturer); Model Catalog: 8.6.07 (Lot serial: contact manufacturer); Model Catalog: 8.5.11 (Lot serial: contact manufacturer); Model Catalog: 8.1.15 (Lot serial: contact manufacturer)