JENNIFER BEARDSALL, et al., Plaintiffs-Appellants, v. CVS PHARMACY, INC., et al., Defendants-Appellees.
No. 19-1850
United States Court of Appeals For the Seventh Circuit
ARGUED JANUARY 15, 2020 — DECIDED MARCH 24, 2020
Appeal from the United States District Court for the Northern District of Illinois, Eastern Division. No. 1:16-cv-06103 — Joan H. Lefkow, Judge.
Before BAUER, EASTERBROOK, and HAMILTON, Circuit Judges.
I. Undisputed Facts and Procedural Background
A. Facts
Defendant Fruit of the Earth, Inc. manufactures aloe vera gel. It both sells the product under its own brand and produces private-label versions for defendants CVS, Walgreens, Walmart, and Target. At issue in this appeal are the Fruit of the Earth and Walgreens products.
The two aloe vera gels are indisputably made from aloe vera plants, though the raw aloe vera harvested by Fruit of the Earth‘s suppliers is processed both before and after being delivered to Fruit of the Earth. The suppliers harvest, fillet, and depulp the aloe vera leaves. The resulting aloe is then pasteurized, filtered with active charcoal to remove color and impurities, treated with preservatives, and dehydrated for shipping. Fruit of the Earth then reconstitutes the dehydrated aloe and adds stabilizers, thickeners, and preservatives to make the final gel product shelf-stable. The parties agree that the products are 98% aloe gel (the reconstituted aloe vera solids) and 2% other ingredients (stabilizers and preservatives).
The only relevant difference between the products is the labeling. Both labels describe the respective products as aloe vera gel. Both also indicate that the products can be used to treat dry, irritated, or sunburned skin. The Fruit of the Earth label calls the product “Aloe Vera 100% Gel” and “100% Pure Aloe Vera Gel.” An asterisk after “100% Gel” leads to information on the back of the label: “Plus stabilizers and preservatives to insure [sic] potency and efficacy.” Each label contains an ingredient list showing that the product contains aloe juice and various other substances. The two labels are reproduced in the attached appendix.1
B. Procedural History
Plaintiffs filed state-law consumer deception claims against Fruit of the Earth, CVS, Walgreens, Walmart, and Target alleging that the labeling of the aloe vera gels — manufac-tured by Fruit of the Earth and sold under all of the defendants’ brands — was misleading. The district court adopted a bifurcated approach to discovery, allowing fact discovery for the Fruit of the Earth and Walgreens products to proceed and staying litigation over the others. The court then set a deadline for class certification, Daubert motions, and dispositive motions.
II. Analysis
We review a grant of summary judgment de novo, taking the facts in the light most favorable to the non-moving parties. Suchanek v. Sturm Foods, Inc., 764 F.3d 750, 761 (7th Cir. 2014). Summary judgment is appropriate “if the movant shows that there is no genuine issue of material fact and the movant is entitled to judgment as a matter of law.”
A. Legal Standard
Plaintiffs have brought claims under fourteen consumer protection statutes spanning twelve different states.2 These statutes all require plaintiffs to prove that the relevant labels are likely to deceive reasonable consumers. See, e.g., Suchanek, 764 F.3d at 756–57 (applying California, Illinois, New Jersey, and New York law, among others); Fink v. Time Warner Cable, 714 F.3d 739, 741 (2d Cir. 2013) (applying California and New York law).
A label is deceptive if it is likely to mislead a reasonable consumer in a material respect, even if it is not literally false. Suchanek, 764 F.3d at 762, citing Williams v. Gerber Prods. Co., 552 F.3d 934, 938 (9th Cir. 2008), and Kraft, Inc. v. FTC, 970 F.2d 311, 314 (7th Cir. 1992) (applying Federal Trade Commission Act,
B. Theories of Deception
Plaintiffs present three distinct but closely related theories of deception. First, they say it is misleading for defendants to call the products “aloe vera gel” because they have only low concentrations of acemannan. Second, they say the labels are misleading because the products do not provide the therapeutic effects that one would expect from a product marketed as aloe vera gel. And third, they say the Fruit of the Earth label is particularly misleading by referring to the product as “Aloe Vera 100% Gel” and “100% Pure Aloe Vera Gel.” We address each theory in turn.
1. Acemannan Concentration and Aloe Vera Gel
Plaintiffs argue primarily that defendants’ labels are deceptive because the products do not contain enough acemannan to be marketed as “aloe vera gel.” Acemannan is a polysaccharide found in aloe vera. No reasonable consumer, plaintiffs argue, would purchase an aloe vera product that contains low concentrations of what plaintiffs maintain is an important therapeutic component.
That might be a viable theory, at least in theory. The problem here is that plaintiffs have not presented any actual evidence that the label is likely to mislead consumers about the nature or quality of the product. Summary judgment is the proverbial “‘put up or shut up’ moment in a lawsuit, when a party must show what evidence it has that would convince a trier of fact to accept its version of events.” Johnson v. Cambridge Indus., Inc., 325 F.3d 892, 901 (7th Cir. 2003). In this case, plaintiffs needed to offer evidence that reasonable consumers were likely to be misled in a material way. Suchanek, 764 F.3d at 762; see also Eli Lilly & Co. v. Arla Foods, Inc., 893 F.3d 375, 382 (7th Cir. 2018) (applying Lanham Act: “the plaintiff ordinarily must produce evidence of actual consumer confusion in order to carry its burden to show that the challenged statement has ‘the tendency to deceive a substantial segment of its audience‘“), quoting Hot Wax, Inc. v. Turtle Wax, Inc., 191 F.3d 813, 819–20 (7th Cir. 1999). Plaintiffs have presented no evidence that acemannan concentration itself is actually salient to consumers. Compare Suchanek, 764 F.3d 753–54 (survey evidence showed
Evidence of the acemannan concentration in defendants’ products — or of the raw aloe vera used to produce them — is not enough if the evidence does not give us reason to believe that consumers care about acemannan concentration. The aloe sold to Fruit of the Earth contained 1.01% acemannan by dry weight. Plaintiffs’ expert testified that fresh aloe — the raw ingredient, not the final product — should contain at least 5% acemannan by dry weight, pointing to a trade organization‘s standards. Testing on the defendants’ final product indicated correspondingly lower concentrations of acemannan in the final product compared to what the expert expected in an aloe product containing undiluted aloe juice.4
Defendants challenge the admissibility of the expert report providing that data, but this evidence makes no difference. Even if the products contained relatively low amounts of acemannan, there is a critical gap in the evidence. Plaintiffs’ expert never testified that a product with lower acemannan concentration cannot fairly be described as aloe. He also offered no opinion on the relationship between aloe concentration and efficacy. Indeed, plaintiffs failed in their briefing and at oral argument to point us to any scientific evidence, inside or outside the record, regarding the level of acemannan needed to render an aloe vera product effective, whatever that might mean.
The deposition testimony presented by plaintiffs cannot fill this evidentiary gap. Some of the plaintiffs testified that they found the labeling to be misleading, particularly regarding the characterization of the product as “100% Pure Aloe Vera Gel.” They said nothing about the acemannan content of the products, however. Rather, they all felt misled because they were incorrectly informed by their lawyers that the products contain little or no aloe vera. This was all based on the factually inaccurate theory that plaintiffs later had to abandon.
To survive summary judgment, plaintiffs needed to offer evidence that consumers were materially misled. They did not. As a result, plaintiffs’ reliance on Suchanek, 764 F.3d 750, Kraft, 970 F.2d 311, and Al Haj v. Pfizer, Inc., No. 17 C 6730, 2019 WL 3202807 (N.D. Ill. July 16, 2019), is not only misplaced but illustrates precisely how their evidence is lacking. In each of those cases, unlike this one, at least some extrinsic evidence was offered to show how
In Suchanek, a manufacturer sold coffee pods for use in a Keurig machine. The pods contained instant coffee rather than the high-quality roasted ground coffee beans that consumers expected. 764 F.3d at 752–53. The front of the package claimed that the pods contained “naturally roasted soluble and microground Arabica Coffee” made with high-quality coffee beans. Id. at 753. The product, however, was more than 95% instant coffee. The plaintiffs in Suchanek offered three surveys showing that consumers expected one product (roasted and ground coffee beans) and received something different that they viewed as inferior (instant coffee). Id. at 753–54. We reversed summary judgment because the surveys created a genuine issue of material fact as to whether the defendant‘s packaging was likely to mislead reasonable consumers. Id. at 762.
In Kraft v. FTC, we upheld an FTC order finding that Kraft misrepresented the amount of calcium contained in Kraft cheese singles. 970 F.2d at 313. The relevant advertising campaign told consumers that Kraft singles were more expensive than competing cheese slices because they were made using five ounces of milk instead of cheaper ingredients. Id. at 314. While five ounces of milk went into one Kraft single, 30% of the calcium contained in the milk was lost during processing. Kraft‘s advertisements implied that one Kraft single provided the same amount of calcium as five ounces of milk.
We found substantial evidence supporting the FTC‘s conclusion that reasonable consumers would be misled about the calcium content of the product. 970 F.2d at 322. We did not require extrinsic evidence of deception, but that was because we credited the expertise of the FTC, and the misleading nature of the challenged claim “was reasonably clear from the face of the advertisement.” Id. at 319; see also id. (“Were this a Lanham Act case, a reviewing court in all likelihood would have relied on extrinsic evidence of consumer perceptions.“). But in affirming the FTC‘s order, we relied on survey data to establish that the deception was material, that is, that consumers placed great importance on calcium consumption and that exaggerated calcium content affected consumers’ decisions to buy Kraft singles. Id. at 323.
In Al Haj v. Pfizer, Inc., Judge Feinerman denied summary judgment for defendants on a claim that a label for “Maximum Strength” cough syrup was misleading. The plaintiffs offered evidence that, as compared to the “Regular Strength” version, the “Maximum Strength” product contained a similar or lower active ingredient concentration (depending on the ingredient), twice the dosage volume, and therefore half the number of doses per bottle. 2019 WL 3202807, at *2. Pfizer historically charged consumers more for the “Maximum Strength” version and continued this pricing structure even after it reformulated the medicine to weaken the more expensive “Maximum Strength” version. Id. at *1–2. Pfizer‘s own market research indicated that “quite a few” customers would be willing to spend more money on “Maximum Strength” medicine because they perceived it to work better and to provide more value. Id. at *3. And the named plaintiff herself testified that she believed that the more expensive product she purchased would be more effective. The court denied Pfizer‘s motion for summary judgment because the language “Maximum Strength” invited customers to assume that, when considering the products side-by-side, the more expensive “Maximum Strength” had a greater concentration of maximum ingredients and more potency per volume than “Regular Strength.” Id. at *5. But the product was
In Suchanek, Kraft, and Al Haj, the plaintiffs identified precisely how the manufacturers’ advertising was misleading and provided evidence that the misrepresentation mattered to consumers. Plaintiffs here, in contrast, have offered no evidence that the products fell short of consumers’ expectations in any material way. This is not to say that extrinsic evidence in the form of consumer surveys or market research is always needed for a plaintiff to survive summary judgment or judgment as a matter of law on a deceptive advertising claim. See, e.g., Schering-Plough Healthcare Products, Inc. v. Schwarz Pharma, Inc., 586 F.3d 500, 512 (7th Cir. 2009) (under Lanham Act, “a representation may be so obviously misleading that there is no need to gather evidence that anyone was confused“). But such evidence is necessary where the advertising is not clearly misleading on its face and materiality is in doubt.
Despite this absence of evidence, plaintiffs argue that the issue of whether a label is misleading is a question of fact that must proceed to a jury. Courts must be careful at summary judgment to view the evidence in the light most favorable to the plaintiff and must send the case to a jury whenever a genuine dispute of material fact exists. See Suchanek, 764 F.3d at 762. But granting summary judgment is appropriate if no reasonable jury could find that defendants’ labels are likely to mislead reasonable consumers. See Fink, 714 F.3d at 741. Plaintiffs here have not gone beyond the pleadings and supported their claims with the necessary evidence. Warsco, 258 F.3d at 563.
Plaintiffs also suggest that their burden to produce “evidence of what reasonable consumers believe” the label to mean is “nonsensical.” Not so. The burden we invoke here simply reflects the burden of production and persuasion borne by plaintiffs in almost all civil litigation. Marion v. Radtke, 641 F.3d 874, 876 (7th Cir. 2011), citing Director, OWCP v. Greenwich Collieries, 512 U.S. 267 (1994).
Plaintiffs also say that summary judgment was inappropriate because the lawsuit was in the “class certification phase.” We reject this argument. Plaintiffs bear no less of a burden at summary judgment simply because the district court set the same deadline for class certification and summary judgment motions. Where plaintiffs intend to rely on market survey evidence to prove deception, rather than their individual impressions and circumstances, that method of proposed proof may be highly relevant in deciding whether to certify a plaintiff class. To decide only class certification in a consumer deception case, it may not be necessary for the market surveys to be complete and in the record. The issue at class certification is whether plaintiffs intend to try to prove their case on the merits through evidence common to class members. Whether (later) survey evidence is admissible and probative can be decided on the merits, and of course, a certified class can lose on the merits of its claims. E.g., Schleicher v. Wendt, 618 F.3d 679, 685 (7th Cir. 2010). As a response to a motion for summary judgment, however, a promise to come forward with more evidence soon is not sufficient. A party who needs more time for necessary factfinding should file a Rule 56(d) motion. Plaintiffs did not do that here.
2. Therapeutic Efficacy
Plaintiffs next argue that the defendants’ labels are misleading because the products “have little or no therapeutic benefit” due to their lack of acemannan and cannot be used effectively for their stated purposes. We do not know whether that is correct, but the problem is that plaintiffs have presented no evidence that the products
Facing this dearth of evidence, plaintiffs ask us to shift the burden to the defendants to prove that their products are effective. But in private consumer deception claims, the plaintiff bears the burden of proving the defendant‘s advertising claim is false or misleading. Private individuals — unlike the Federal Trade Commission — may not bring an action without supporting evidence and merely demand that the defendant prove the claim it makes for its products. Compare Kwan v. SanMedica Int‘l, 854 F.3d 1088, 1096 (9th Cir. 2017) (under California false advertising law, plaintiffs “do not have the power to require defendants to substantiate their advertising claims“), citing National Council Against Health Fraud, Inc. v. King Bio Pharmaceuticals, Inc., 107 Cal. App. 4th 1336, 1344 (2003), with FTC v. Pantron I Corp., 33 F.3d 1088, 1096 (9th Cir. 1994) (FTC may rely on theory that advertiser lacked reasonable basis for its claims).
3. “100% Pure” and Ambiguity
Plaintiffs’ last theory of deception centers on the Fruit of the Earth label‘s description of the product as “Aloe Vera 100% Gel” and “100% Pure Aloe Vera Gel.” As best we can tell, plaintiffs think these phrases are misleading in two ways.
First, plaintiffs say these statements misrepresent the quality of the product by giving consumers the impression that the product is “high quality” or “especially effective” aloe when it is not. But this is just a variant on the argument that the products cannot be called aloe vera gel, and it fails for the same reasons. Plaintiffs have presented no evidence indicating that consumers interpret these as statements of quality. Just as they have presented no evidence showing that some amount of acemannan is needed to call a product aloe vera, they have presented no evidence that some amount of acemannan is needed to call an aloe vera product “100% pure.”
Second, plaintiffs suggest that the label is misleading because the product contains preservatives and stabilizers and is therefore not “100% Pure Aloe Vera Gel.” Specifically, plaintiffs object to the district court‘s conclusion that the “100% Gel” and “100% Pure” statements were ambiguous with respect to the presence of stabilizers and preservatives such that the statements could be clarified by the ingredients list. But plaintiffs conceded in their summary judgment brief and deposition testimony that “the presence of preservatives — in reasonably small amounts — was acceptable and something they expected,” and that “[n]o [p]laintiff took the label to mean that there was absolutely nothing other than aloe vera in the bottle.”5 The presence of other substances in the product — and the disclosure of those products in the ingredients list — is therefore irrelevant to the theories plaintiffs have chosen to pursue. We are skeptical of defendants’ position at oral argument that an asterisk pointing to an ingredient list in fine print could save virtually any deceptive slogan claiming purity. Given plaintiffs’ arguments and testimony, though, we need not decide here whether “100% Pure Aloe Vera Gel” is ambiguous with respect to the presence of stabilizers and preservatives.
Along similar lines, plaintiffs say that the district court erred in considering
The judgment of the district court is
AFFIRMED.
