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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Using the rt chart function in aria versions 8.0 and 8.1 when users select the "convert to set-up field" option a set-up field is created that removes the dmlc (dynamic multi leaf collimator) plan components in order to create an open collimator for field light setup purposes. in a recently reported case a user having selected this option in error then converted the set- up field back to a treatment field. the resulting treatment field is then missing the dmlc. if this error is not detected prior to patient treatment open field treatment can result.
Model Catalog: (Lot serial: HIT2414M); Model Catalog: (Lot serial: HIT0606M); Model Catalog: (Lot serial: HIT0040); Model Catalog: (Lot serial: HIT2414R1); Model Catalog: (Lot serial: HIT0606R1)