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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It has been seen that the collimator jaw settings defined a radiation field that was not completely within the shielded area of the conical accessory. when this happens radiation may be delivered outside the area shielded by the conical collimator potentially resulting in an unintended radiation dose to patients which could result in patient injury.