This is something I don't get. How do you figure they could ever enforce a ban? They can't ban the ingredients to ejuice...they can't ban lithium batteries, kanthal wire, and electronics parts. An e-cigarette isn't exactly a high-tech device.
And what about the rest of the world? You think the USA is going to tell China to stop producing e-cig products? HAH!
I mean, banning us from vaping in public spaces is one thing, but completely banning vaping? Absurd!
I really dislike the fact that people are throwing the word "Ban" out there. You're providing an easy strawman.
The FDA is NOT proposing to ban anything.
They are proposing to prevent the sale of items which have not been approved. Getting an item approved will cost (by the FDA's estimate) about $334,000. Their definition of a product is that if ANY component of that product is different, its a separate product.
Moo Juice at 20/80 3 mg is a product
Moo Juice at 40/60 3 mg is a separate product
Moo Juice at 20/80 6 mg is a separate product
And so forth. In fact, anything that has a different SKU is a different product. A blue EVOD head is a different product than a green one.
And YES, they DO intend to cover heads and mods as well; the proposed deeming regulations make that clear. Whether or not vendors could get around this by re-labeling hardware is unknown; the verbiage includes "Or could be used" which leaves the door wide open for them to demand registration and approval of these as well, and to seize shipments of hardware even though there is absolutely no tobacco or nicotine in them.
Absurd? Yes. Happening? Yes.
Edit: And merely applying for approval, and paying the costs to do so is no guarantee that the FDA will actually grant that approval, or when, if ever, they will even look at the application. There are no mandates to the FDA that they must act on these, no formal guidelines on what information must be included in the application (and if the FDA decides you didn't provide enough info, the application gets rejected without recourse. Back to square 0).
Lest you think that's farfetched, look at the backlog of applications since the FDA first was able to require them. IIRC there are over 3000 earlier applications from 2007 that the FDA hasn't responded to in any way, and the number it has actually acted on is on the order of 20. And most of these were SE applications, which are MUCH simpler and cheaper, but not available for e-cig products.) Oh, and most of the "actions" were rejecting the application for insufficient evidence provided.
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