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this post was submitted on 26 May 2025
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You would think so, right? But that doesn't have a requirement ID so apparently it can't be referenced in the incident report.
Sounds like the devs are cowards. Or maybe their pay counts on it not being a bug
Software for a medical device. Everything needs to be done exactly right and documented in three different places or else the regulatory agencies from at least three countries get really angry at you and worst case pull your device from circulation. Less cowardice and more cover your ass. Still annoying though.
I see, so it's a situation where catching the full blame can tank your career. Yeah, that makes sense.