Lanovaz filed a putative class action under the UCL, FAL,
CLRA, Song-Beverly Act, and Magnuson-Moss Warranty Act, based on claims that
Twining’s green tea was allegedly misbranded.
The box label describes the tea as a “natural source of antioxidants.”
Lanovaz alleged that Twinings was making unlawful nutrient content claims,
unlawful antioxidant claims, unlawful/unapproved health claims, and unlawful
disease prevention/treatment claims.
Twinings moved to strike claims about statements Lanovaz
didn’t see and products she didn’t buy, since she only bought the 1.41 oz. box
of Green Tea and didn’t specifically identify other products or other
information on which she relied, despite references to buying other Twinings
products and viewing its website. In general, a person can’t expand claims to
include products not purchased or ads not relied on. Acknowledging the judicial
split on the issue, the court held that there could be no injury, as required,
where the plaintiff didn’t herself buy the product at issue. So she could only proceed based on the green
tea product bearing the label “natural source of antioxidants.” (I assume she’s allowed to represent those who
bought 4 oz. boxes … or is she?)
Twinings then argued that her claims were preempted by the
FDCA/NLEA. Lanovaz rejoined that she was
suing under California state law, which adopts rules identical to those of the
FDCA/NLEA/FDA regulations, something specifically allowed by the NLEA’s preemption
provisions. Twinings relied on Pom
Wonderful LLC v. Coca–Cola Co., 679 F.3d 1170 (9th Cir. 2012), where the Ninth
Circuit barred a Lanham Act claim against a label that apparently was
authorized under FDA regulations. If the
FDA declined to impose labeling requirements, the Lanham Act couldn’t do
so. Pom
was inapposite. First, it wasn’t about
state law claims and indeed remanded the UCL/FAL claims to the district
court. The NLEA has been repeatedly
interpreted not to preempt state law requirements that parallel or mirror the
NLEA. “[T]he purpose of the NLEA is not
to preclude all state regulation of nutritional labeling, but to prevent State
and local governments from adopting inconsistent requirements with respect to
the labeling of nutrients.”
So the question was whether Lanovaz was seeking to enforce
the FDA regulations, incorporated into California law, or whether she was
asserting claims beyond what the regulations require. The difficult question
was whether “natural source of antioxidants” was a federally regulated nutrient
content claim. A claim that expressly or
implicitly characterizes the level of a nutrient of a type required to be in
the nutrition labeling is a regulated nutrient content claim. Twinings argued that “natural source” didn’t
characterize the level of antioxidant.
Under the regulations, an antioxidant nutrient content claim can be used
when there’s a reference daily intake for the nutrient, the nutrient has
recognized antioxidant activity, the level of the nutrient was sufficient to
qualify for the claim, and the names of the nutrients were included. Twinings’ “natural source of antioxidants”
label didn’t meet those requirements. So
if it was a nutrient content claim, the state UCL/FAL claims were viable.
The FDA hasn’t officially defined “source of” or “natural
source of” as making a nutrient content claim, but it has identified similar
terms such as “excellent source of,” “good source of,” “contains,” and
“provides” as the operative words in nutrient content claims. In a 2011 warning letter, it advised that
claims using “source” were nutrient content claims. Thus, the court found that the allegations of
the complaint sufficed to set forth a nonpreempted claim.
Twinings also challenged Lanovaz’s Article III standing. It
argued that she got tea that didn’t injure her in any way. Lanovaz responded that she was misled into
buying the tea, and buying a product you wouldn’t otherwise have bought is an
economic injury in fact. Whether she was
actually misled was a factual question.
Twinings argued that her claim to rely on a
“hyper-technical” violation of FDA regulations was implausible. Lanovaz alleged that she thought she was
buying tea that met the minimum threshold to make an antioxidant claim, and
that buying healthy products was important to her. But, Twinings contended, the statement was
literally true and a reasonable consumer wouldn’t know that the FDA has defined
“source”/“natural source,” so they’re not meaningful. The court found the allegations
plausible. (I think it’s clearly
plausible to have a general belief that the government regulates product claims
and thus wouldn’t allow them if they don’t meet a minimum threshold, even if
you don’t know the numerical etc. details of those regulations.)
However, the Song-Beverly Consumer Warranty Act claim failed
because the Act exempts consumables, which the tea is. The Magnuson-Moss Act claim also failed
because the “natural source” claim wasn’t a warranty against a product defect.
And the unjust enrichment/restitution claim failed as superfluous/duplicative
of statutory claims.
2 comments:
What with vaporizing the value of plaintiff's $8.2M of marketing since 2009 and opening up a nascent market for zirconia crowns to copycat dental labs from India to China, I can hear businesses gnashing their teeth over this decision.
And, for what? Will future competitors really feel constrained to add a letter or three to the beginning of the allegedly infringing word "bruxer" --e.g., Z-Bruxer crowns?
And, what possible value is there in providing one of a 1,000 possible surveys in a matter where the root of the matter is genericness of the mark when the plaintiff can prove actual confusion?
Did the defendant have survey to show genericness? If nothing else, this looks like a case that should have gone to the jury. Based on the sarcastic opening of the opinion it sounds like the judge has a problem with dentists that he took it out on the plaintiff.
Note: I'm pretty sure anonymous meant to comment on a previous post. As always, comments reflect the opinion of the commenter, not mine.
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