Rad onc recall.
In this analysis of FDA recalls of radiation oncology related-equipment between 2010 and 2016, the majority of all recalls were related to linear accelerators or their control software. There was a spike in reporting of such issues following the notorious 2010 radiation overdosing incident relating to collimator settings. In fact, recalls related to wrong dose, volume, or targetting represented 75% of all recalls. Compared to hardware recalls, control software recalls were 4 times more likely to be associated with incorrect dose or target events. | Jairam, Pract Radiat Oncol 2019
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