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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Philips has become aware that under very specific error conditions the system may execute an unintended exposure: - the hand switch is erroneously stuck in pressed position while the system is switched off - the system is powered up with the hand switch in that erroneous condition - the user logs in selects a patient for examination gets a green ready light in the examination context if the tube arm is then moved out of the zero position the system is doing an exposure.