this post was submitted on 07 Mar 2024
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There must be wrinkles to the two processes that are a little counter intuitive then. And certainly ones I'm not familiar with.
I think it's more that the company knows exactly what, how much of and how a harmful product gets into their product.
If the FDA issues an involuntary recall, they have to figure out the structure of the company and supply chain, identify every step and process, and make sure a company complies fully.
Effectively, the result is the same, but it's a much simpler and quicker process if the company shows the FDA what happened, how it happened and where target than the FDA having to identify every process of every harmful product.
Many companies do care about the health of their customers and want to make a better product.
Practically, are you going to be the cinnamon company that said "nah, we think the lead won't hurt our customers" and face severe penalties, lose all your customers and suffer what is likely a permanent now to your professional and personal reputation?
It's a simpler matter and better for business (sick people and dead people buy fewer products) to identify the problem, fix it and continue business as usual, while looking responsible and ethical.
Interesting, thanks for the extra info.
For sure, I always like learning