Sheiner v. Supervalu Inc.

CourtDistrict Court, S.D. New York
DecidedMay 28, 2024
Docket7:22-cv-10262
StatusUnknown

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

Bluebook
Sheiner v. Supervalu Inc., (S.D.N.Y. 2024).

Opinion

DOCUMENT ELECTRONICALLY FILED UNITED STATES DISTRICT COURT DOC #: SOUTHERN DISTRICT OF NEW YORK DATE FILED: 05/28/2024 JESSE SHEINER, individually and on behalf of all others similarly situated, No. 22 Civ. 10262 (NSR) Plaintiff, OPINION & ORDER -against- SUPERVALU INC., Defendant.

NELSON S. ROMAN, United States District Judge Plaintiff Jesse Sheiner (“Plaintiff’) brings this action, on behalf of himself and all others similarly situated, against Defendant Supervalu Inc. (“Defendant”), for (1) violations of Sections 349 and 350 of the New York General Business Law (“GBL”); (2) violation of “state consumer fraud acts”; (3) breach of express warranty, implied warranty of merchantability/fitness for a particular purpose, and the Magnuson Moss Warranty Act (“MMWA”); (4) fraud; and (5) unjust enrichment. (Amended Complaint “Am. Compl.,” ECF No. 12, §§ 88-116.) Defendant moves to dismiss Plaintiff's Amended Complaint under Federal Rule of Civil Procedure 12(b)(6). (the “Motion”, ECF No. 16.) For the following reasons, Defendant’s Motion is GRANTED in part and DENIED in part. BACKGROUND I. Factual Background The following facts are taken from the Amended Complaint and assumed to be true for the purposes of Defendant’s Motion. Defendant sells a lidocaine patch product (the “Product”). (Am. Compl. ¥ 1.) The Product’s front label describes it as “Maximum Strength Lidocaine Patch” product which contains “topical

anesthetic 4% Lidocaine” which “desensitize[s] aggravated nerves” to provide “temporary relief of pain” to the “back, neck, shoulders, knees, elbows” for “up to 8 Hours of relief.” (Id. ¶¶ 1-2.) The front label also incorporates that statement “compare to Salonpas® Lidocaine Patch active ingredient” (Id.) Plaintiff alleges that, when purchasing the Product, he was misled by the

following statements: “Up to 8 Hours Numbing Relief”. Plaintiff asserts that consumers understand this phrase to be a promise that the Product will adhere to a consumer’s body and provide maximum strength pain relief for “no less than eight hours.” (Id. ¶ 29.) As support, he refers to the “Directions” section on the back label of the Product, which instructs that a consumer should “apply 1 patch at a time to affected area, not more than 3 to 4 times daily” and “remove patch from skin after at most 8 hours of application.” (Id. ¶¶ 30-31.) He alleges that the Product “is unable to adhere to skin for more than four hours, often peeling off within minutes of light activity.” (id. ¶ 32) and “did not reliably adhere to Plaintiff’s body for anywhere close to eight hours, which prevented it from providing even temporary pain relief” (id. ¶ 76). Plaintiff also bases this claim on the results of a

study by the Journal of Pain Research. (Id. ¶¶ 21-25, 32, 37, 52.) “Maximum Strength”. Plaintiff alleges that the Product is not “Maximum Strength” because “prescription lidocaine patches exist on the market that deliver greater amounts of lidocaine to the user.” (Id. ¶ 35.) Plaintiff alleges the statement inviting consumers to “compare to Salonpas® Lidocaine Patch active ingredient” further contributes to this confusion because the Product “contains roughly forty percent less lidocaine” than found in the Salonpas® OTC Lidocaine Patch product. (Id. ¶ 41.) “Numbing Relief”. Plaintiff alleges the phrase “numbing relief” implies the OTC Product provides relief associated with “medical treatments requiring a prescription and FDA approval.” (Id. ¶ 47.) He also alleges this phrase “implies [the Product] will completely block and numb nerves and pain receptors, eliminate responses to painful stimuli, and can treat neuropathic and musculoskeletal pain, including back pain.” (Id. ¶ 45.) Plaintiff purchased the Product at locations including Walmart, Walgreens, and/or CVS

throughout Sullivan and Orange Counties, among other places, between June 2020 and November 2022, or among other times. (Id. ¶ 71.) Plaintiff bought the Product at or exceeding the above- referenced price and allegedly paid more for the Product than he would have had he known the representations and omissions were false and misleading, or would not have purchased it altogether. (Id. ¶¶ 77-78.) II. Procedural History Plaintiff filed the original Complaint on December 3, 2022. (ECF No. 1.) Defendant initially sought leave on April 11, 2023 (ECF No. 8) to bring a motion to dismiss the initial Complaint. Plaintiff responded on April 14, 2023 (ECF No. 10) opposing leave and informing the Court that he would avail himself of his right to amend as a matter of course pursuant to Federal

Rule of Civil Procedure 15(a)(1)(B). The Court, inter alia, directed Plaintiff to file an Amended Complaint no later than May 11, 2023. (ECF No. 11). Plaintiff then filed an Amended Complaint on May 11, 2023. (ECF No. 12.) On September 28, 2023, Defendant filed the instant Motion (ECF No. 16), as well as a memorandum of law (“Def.’s MoL”, ECF No. 17) and reply (“Def.’s Reply”, ECF No. 20), in support thereof. Plaintiff filed an opposition to Defendant’s Motion. (“Pltf.’s Opp.”, ECF No. 19).

LEGAL STANDARD To survive a motion to dismiss pursuant to Fed. R. Civ. P. 12(b)(6), for “failure to state a claim upon which relief can be granted,” a complaint must “contain 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) (quoting Bell Atl. Corp. v. Twombly, 550 U.S. 544, 570 (2007)). “Although for the purposes of a motion to dismiss [a court] must take all of the factual allegations in the complaint as true, [it is] ‘not bound to accept as true a legal conclusion couched as a factual allegation.’”

Iqbal, 556 U.S. at 678 (quoting Twombly, 550 U.S. at 555). The Court will accept the facts in a complaint as true “and then determine whether they plausibly give rise to an entitlement to relief.” Id. A claim is facially plausible when the factual content pleaded allows the Court “to draw a reasonable inference that the defendant is liable for the misconduct alleged.” Id. at 678. Ultimately, determining whether a complaint states a facially plausible claim upon which relief may be granted is “a context-specific task that requires the reviewing court to draw on its judicial experience and common sense.” Id. at 679. DISCUSSION I. Withdrawn Claims In his opposition papers, Plaintiff withdraws his claims on behalf of the Consumer Fraud

Multi-State Class, and his claims for breaches of the Implied Warranty of Merchantability/Fitness for a Particular Purpose and the MMWA. (Pltf.’s Opp. at 1 n.1.) As a result, these claims are dismissed. II. NY GBL Claims Plaintiff's first cause of action arises under Sections 349 and 350 of the GBL. Section 349 of the GBL provides a cause of action for any person injured by “[d]eceptive acts or practices in the conduct of any business, trade or commerce or in the furnishing of any service.” N.Y. Gen. Bus. Law. § 349(a), (h). “‘Deceptive acts’ are acts that are ‘likely to mislead a reasonable consumer acting reasonably under the circumstances.’” Chufen Chen v. Dunkin’ Brands, Inc., 954 F.3d 492, 500 (2d Cir. 2020) (quoting Fink v. Time Warner Cable, 714 F.3d 739, 741 (2d Cir. 2013)). Section 350 of the GBL prohibits “[f]alse advertising in the conduct of any business, trade or commerce,” and is analyzed under the same “reasonable consumer” standard as Section 349. Id. (citing Maurizio v.

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