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Over the last few years, a series of device recalls were mandated by the FDA for dangerous or defective medical devices. User interface issues were one of the main causes of these recalls. The issues were observed across multiple device manufacturers and device types, and appear to be related to poor device design and engineering. In this seminar, we will discuss user interface issues commonly observed in commercial devices such as infusion pumps, ventilators, and patient monitors. Several concrete examples will be presented that can help staff members to identify latent problems with these devices, as well as solutions to avoid these latent problems. Ultimately, this knowledge is also valuable to inform procurement decisions. The presented work is carried out within the CHI+MED research project (http://www.chi-med.ac.uk), and in collaboration with the US Food and Drug Administration (FDA) with the aim of improving the safety and effectiveness of medical devices. Copyright and disclaimer: the material presented in this page contains information, data, documents, pages and images prepared for training and education purposes. You may copy, distribute, display, download and otherwise freely deal with the material for training and education purpose only. Support: for any technical issues with the video, please email Paolo at [email protected]