Tlaib v. Chattem, Inc.

CourtDistrict Court, N.D. Illinois
DecidedSeptember 8, 2023
Docket1:23-cv-00376
StatusUnknown

This text of Tlaib v. Chattem, Inc. (Tlaib v. Chattem, Inc.) is published on Counsel Stack Legal Research, covering District Court, N.D. Illinois primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Tlaib v. Chattem, Inc., (N.D. Ill. 2023).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE NORTHERN DISTRICT OF ILLINOIS EASTERN DIVISION

MOHAMAD TLAIB, individually ) and on behalf of all others similarly situated, ) ) Plaintiff, ) Case No. 23-CV-376 ) v. ) Judge Robert W. Gettleman ) CHATTEM, INC., ) ) Defendant. )

MEMORANDUM OPINION & ORDER Plaintiff Mohamad Tlaib, on behalf of himself and other similarly situated individuals, brings this first amended complaint against defendant Chattem, Inc. for alleged violations of consumer protection law. Plaintiff asserts claims under the Illinois Consumer Fraud and Deceptive Business Practices Act (“ICFA”), 815 ILCS 505/1, as well as breaches of express warranty, implied warranty of merchantability and fitness for a particular purpose, and unjust enrichment. Defendant moves to dismiss plaintiff’s first amended complaint for failure to state a claim pursuant to Federal Rule of Civil Procedure 12(b)(6) (Doc. 13). For the reasons stated below, the court grants defendant’s motion. BACKGROUND Defendant manufactures, labels, and sells dry mouth lozenges under the ACT brand, which plaintiff purchased from various pharmacies in Cook County. According to plaintiff, defendant manufactured the dry mouth lozenges for purchase and use by individuals affected by xerostomia, or hypofunction of the salivary glands. Plaintiff alleges that individuals with xerostomia are unable to produce saliva, which plays a “significant role in oral health,” and the absence of saliva “significantly increases the risk of dental caries, demineralization, tooth sensitivity, dental erosion, candidiasis, and other oral diseases.” Plaintiff alleges that defendant markets its ACT dry mouth lozenges (“the product”) toward individuals suffering from xerostomia because the product’s front label states that the lozenges “soothe[ ] dry mouth,” “moisturize[ ] mouth tissue,” and “freshen[ ] breath.” On the

label, the lozenges are pictured next to a splash of water. According to plaintiff, the product is intended to “linger in the mouth as long as possible to relieve dry mouth symptoms,” and the lozenges stimulate saliva production, which “provides lubricating effects, increasing comfort and in theory, preventing dental erosion and caries.” On its back label, the “suggested use” instructions state that consumers should “[u]se as needed.” Plaintiff claims that he expected defendant’s product to “improve the symptoms of dry mouth,” and purchased the product “to improve oral health.” Plaintiff alleges, however, that laboratory testing shows that the product has a pH of 5.72,1 which is “below the critical pH of tooth enamel and root dentin.” He cites several academic studies that “highlight[ ] the dangers where the acidity level is not at roughly 6.7 pH or

higher.” Plaintiff complains that low pH values can indicate the immediate erosive potential of a solution, and defendant’s lozenges are associated with a “dentin loss delta mean” of -0.0075, with a 0.004 standard deviation, which is similar to high-acidity products. Plaintiff further complains that instructing consumers to “use as needed” is “counter-intuitive” because the product is acidic, and the target group cannot dilute the product’s pH with saliva. Plaintiff states that he “did not know or expect the Product’s pH meant it contributed to demineralization, dental erosion, sensitivity, and caries.” Plaintiff alleges that the product’s label is actionable because, “[i]n light of the Product’s

1 According to plaintiff, statistical analysis demonstrates that pH is correlated with titratable acidity (otherwise known as “TA”). acidity, it is misleading to market [the product] to individuals suffering from dry mouth because it will have a detrimental effect on oral health.” Plaintiff explains that the product “fails to disclose and omits the likelihood of demineralization, dental erosion, greater tooth sensitivity and higher incidence of dental caries,” and he did not expect the product to “be formulated to

negatively affect oral health” based on its pH level. Instead, plaintiff claims that the product “expressly and impliedly warranted to plaintiff that it would improve oral health and not negatively affect oral health.” He complains that defendant “had actual knowledge of Product’s pH level because it formulated and manufactured it, and its deleterious effects on oral health,” and “had knowledge of the Product’s potential for causing dental erosion.” Further, plaintiff complains that the product “unlawfully claims to ‘mitigate . . . disease” through its effects on salivary gland disorders using lay terminology, namely, “Moisturizes Mouth Tissue.” He complains that he “paid more for the Product, would have paid less or not have purchased it had he known the representations and omissions were false and misleading.” The product was sold for “not less than $6.99 per 36 lozenges, excluding tax and sales.”

LEGAL STANDARD “To survive a motion to dismiss [under Rule 12(b)(6)], a complaint must allege sufficient factual matter, accepted as true, to state a claim to relief that is plausible on its face.” Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009), citing Fed. R. Civ. Pro. 12(b)(6). For a claim to have “facial plausibility,” a plaintiff must plead “factual content that allows the court to draw the reasonable inference that the defendant is liable for the misconduct alleged.” Id. “[W]here the well-pleaded facts do not permit the court to infer more than the possibility of misconduct, the complaint has alleged—but has not shown—that the pleader is entitled to relief.” Id. “Threadbare recitals of the elements of a cause of action, supported by mere conclusory statements, do not suffice.” Id. Claims involving fraud, such as deception claims under the ICFA, are subject to a heightened pleading standard set forth in Rule 9(b). Fed. R. Civ. Pro. 9(b); Camasta v. Jos. A. Bank Clothiers, Inc., 761 F.3d 732, 736 (7th Cir. 2014). Rule 9(b) requires that the plaintiff “state with particularity the circumstances constituting fraud.” Fed. R. Civ. Pro. 9(b). The

Seventh Circuit has interpreted the 9(b) standard to require a plaintiff to “describe[e] the who, what, when, where, and how of the fraud.” Anchorbank, FSB v. Hofer, 649 F.3d 610, 615 (7th Cir. 2011). DISCUSSION Plaintiff brings claims under Illinois state law, and as a federal court reviewing the case under diversity jurisdiction, this court evaluates plaintiff’s claims pursuant to Illinois state law as the Illinois Supreme Court would review them. See Nationwide Agribusiness Ins. Co. v. Dugan, 810 F.3d 446, 450 (7th Cir. 2015). The court begins by evaluating defendant’s motion to dismiss plaintiff’s claim for violation of the ICFA for misleading and deceptive practices.2 According to defendant,

plaintiff’s ICFA theory fails to state a claim because he does not allege a misleading or deceptive statement on the product’s label. Specifically, plaintiff does not allege that the product, which represents that it “soothes dry mouth,” “moisturizes mouth tissue,” and “freshens breath,” failed to soothe his dry mouth, moisturize his mouth tissue, or freshen his breath. Further, assuming that defendant engaged in deception, plaintiff does not allege that a reasonable consumer would be misled or that defendant intended him to rely on its alleged deception. To prevail on a claim under the ICFA, a plaintiff must show: (1) a deceptive act or

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Tlaib v. Chattem, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/tlaib-v-chattem-inc-ilnd-2023.