As a medical device sw developer, if doing your risk analysis, you notice that if for some reason the user miss something important, it will create a risk for t

As a medical device sw developer, if doing your risk analysis, you notice that if for some reason the user miss something important, it will create a risk for the patient, the easiest (and cheap and lazy) solution is often to add a blaring alarm or scary pop-up to ask the user to confirm/check. This way you can say that you have a mitigation, so the FDA is happy, you are happy because you can sell your product. The downside is that it creates a horrible user experience most of the time. This is unfortunate but this is a result of incentives of the different actors. Another slightly related issue is that, you'd rather restrict what you user can do, because you're sure it will be at least safe. So often doctors can be frustrated because the system is not permissive enough. Most of the time, as a vendor, you prefer to sell a clumsy system that facing the risk of having a recall.