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 event occurred with c-series clinac accelerator. the event entails excessive connector resistance which caused the actual jaw positions to differ from the intended jaw positions without warning the operator. normal morning daily quality assurance testing and light field verification detected the discrepancy. investigation found that a similar issue could arise on the gantry or couch axes. this does not affect the mlc.
Model Catalog: TRILOGY (Lot serial: >10 serial numbers.); Model Catalog: TRILOGY (Lot serial: Contact manufacturer); Model Catalog: 23EX (Lot serial: H290285); Model Catalog: 2100C (Lot serial: >10 SERIAL NUMBERS.); Model Catalog: 2100C (Lot serial: CONTACT MANUFACTURER.); Model Catalog: 21EX (Lot serial: >10 serial numbers.); Model Catalog: NOVALIS TX (Lot serial: ); Model Catalog: CLINAC IX (Lot serial: Contact manufacturer.); Model Catalog: CLINAC IX (Lot serial: >10 Serial numbers.); Model Catalog: 21EX (Lot serial: Contact manufacturer.); Model Catalog: 6EX (Lot serial: >10 serial numbers.); Model Catalog: 600C (Lot serial: >10 serial numbers.); Model Catalog: 600N (Lot serial: >10 serial numbers.); Model Catalog: 6EX (Lot serial: Contact manufacturer.); Model Catalog: 600C (Lot serial: Contact manufacturer.); Model Catalog: 600N (Lot serial: Contact manufacturer.)