It’s class III medical device software
It looks like the advisory/recall notice came out (depending on time zones) either before his posts or shortly thereafter.
Looks like the company has jumped on this right away as they should.
They have several non app solutions for bolus dosing. Looks like the app is new (iOS version isn’t even out yet) and they didn’t vet their consultants output adequately. Probably because this was some quick port that was outsourced and management didn’t pay attention because ‘requirements are the same’.
Super important in med device development to have adequate internal oversight of developers to ensure requirements are properly rigorously tested. Especially in a class III device like this
I’ve recently had the opposite: code worked then the next day without anything changing it didn’t.
Turned out the J-Link programmer always needs the license check to work, but that expires every day at midnight. It only prompts again if you choose the app and restart it. So I couldn’t get my debugger to work and spent hours trying to figure it out until I did the best thing. I turned it off and on again.
I felt kinda bad about how all my private repos prevent me from flexing. But then he got to the last one and let me say - as a part-time farmer coder who just picked a ripe plum off my tree, I’m better than y’all
I knew the memes would be coming after this moment
I’ve used it in the past when having flash memory blocks that could change but you need the compiler to put them into flash memory and not RAM. It’s mainly to get the compiler to stop assuming that it can optimize using the default value.