Agee v. The Kroger Co.

CourtDistrict Court, N.D. Illinois
DecidedApril 19, 2023
Docket1:22-cv-04744
StatusUnknown

This text of Agee v. The Kroger Co. (Agee v. The Kroger Co.) 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
Agee v. The Kroger Co., (N.D. Ill. 2023).

Opinion

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

TIFFANY AGEE, ) individually and on behalf of all ) others similarly situated, ) ) Plaintiffs, ) ) vs. ) Case No. 22 C 4744 ) THE KROGER CO., ) ) Defendant. )

MEMORANDUM OPINION AND ORDER

MATTHEW F. KENNELLY, District Judge: Tiffany Agee filed suit against The Kroger Company. Kroger markets and sells over-the-counter (OTC) adhesive patches containing lidocaine, a topical anesthetic used to treat pain symptoms. Agee alleges that the product's labeling is misleading in a number of ways. She asserts claims individually and on behalf of a proposed multi- state class under the Illinois Consumer Fraud and Deceptive Business Practices Act (ICFA) (Count 1) and the state consumer fraud acts of various states listed in the complaint (Count 2). Agee also asserts claims, individually and on behalf of the proposed class, for breach of warranty (Count 3); negligent misrepresentation (Count 4); common law fraud (Count 5); and unjust enrichment (Count 6). Kroger has moved dismiss the complaint under Federal Rule of Civil Procedure 12(b)(6) for failure to state a claim and under Rule 12(b)(1) for lack of subject matter jurisdiction. For the reasons stated below, the Court dismisses counts 3 and 5 and strikes Agee's request for injunctive relief but otherwise denies Kroger's motion. Background The Court takes the following facts from the allegations in Agee’s complaint. Kroger is an Ohio corporation that operates a chain of supermarkets and distributes its own "generic" or "store brand" private-label products. These products are manufactured by third parties and sold under the Kroger name. The lidocaine patches at issue in this case are one such product. Agee alleges that between June 2021 and November 2021, she purchased the product at issue at locations including Food 4 Less, a store located at 4821 W. North Avenue in Chicago. In support of its motion to dismiss, Kroger submitted a copy of the front and back of the product packaging: pee CM Cr eee Lae a lel tot oo

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Drug Facts Active ingredient Purpose Lidocaine □□□ nnn ee ee ee ee ee eee =. pica anesthetic Uses Warnings For extemal use only Do not use Mimore than | patch atatime lion wounds or damaged skin li with a heating pad if you have ever had an allergic reaction to this product or any of its ingrediants When using this product Muse only as directed Mizvold contact with the eyes, mucous membranes or rashes Wido not bandage tightly Stop use and ask a doctor if Mibcalzed skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering conditions worsen Msymptoms persist for mare than 7 days Misymptome clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional betore use, Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Canter right away (1-200-222-1222), Soe Adults and children 12 years of age and ower: Mickan and dry affected area remove film trom patch and apply to the skin (see MBustration| apply 1 patch ata time to affected area, not more than 3 to 4 times daily remove patch from the skin afier at most & hours of application Children under 12 years of age: consult a doctor Mavoid storing product in direct suniight Mprotect product from excessive motsture Mistore at 20-25°C (62-77°F) Inactive ingredients carboxymethyicellulose sodium, dihydroxyaluminum aminoacetata, edatate disodium, glycerin, kaolin, methylparaben, polyacrylic acid, polyvinyl alcohol, propylene glycol, propyiparaben, purified water, sodium polyacrylate, sodium polyacryfate starch, sorbitol solution, tartaric acid, urea

Def.’s Mot. to Dismiss, Ex. A. Agee alleges that the label misleadingly promises "Up to 8 Hours of Relief," at "Maximum Strength," and that the patch can be used "For Temporary Relief of Pain," to "Desensitize Aggravated Nerves,” and for "Numbing Relief." Compl. {J 3, 25. The alleged misrepresentations fall into three categories. First, Agee contends that the package label's use of the phrase "Up to 8 Hours of Relief" is misleading

because, she alleges, the patch regularly peels off the bodies of users within a few hours of being applied and often with minutes of application, thus limiting the amount of relief it provides. Id. ¶ 16. In support of this contention, Agee points to a report by the Food and Drug Administration (FDA) that found that "approximately 70% of concerns

stemming from lidocaine patches involve their poor adhesion," id. ¶ 9, as well as a peer- reviewed study published in January 2021 by the Journal of Pain Research. Agee alleges that the study determined that "0% of generic prescription lidocaine patches had a >90% adhesion rate to the study's subjects after 12 hours, i.e., essentially no part of the product lifting off the skin." Id. ¶ 10. The study also allegedly found that "a newly developed 1.8% lidocaine patch technology, which is bioequivalent to 5% lidocaine patches, maintained a mean adhesion >90% across all time points." Id. ¶ 13. Agee acknowledges that the study tested only generic prescription lidocaine patches, but she alleges that Kroger's product, "which has not undergone rigorous approval process required by the FDA and use[s] the same outdated and defective adhesion technology

as the generic lidocaine patches, fare[s] no better." Id. ¶ 14. Agee alleges that Kroger's use of the phrase "Up to 8 Hours" on its label leads consumers to expect that the product will remain applied for "no less than eight hours or even longer." Id. ¶ 17. Agee also alleges that the "[d]irections confirm the Product will adhere to the user's skin for the full eight hours" because the package instructs the user to remove the patch "after at most 8 hours of application." Id. ¶ 18. Because the product does not adhere to the skin for eight hours (thus diminishing its ability to relieve pain), Agee alleges, this instruction on the back of the product–as well as the phrase "Up to 8 Hours of Relief" on the front of it–are themselves misleading and also render misleading the representation "Maximum Strength." Next, Agee alleges that the term "Maximum Strength" is misleading for two additional reasons. First, she alleges that because the amount of lidocaine delivered by the patch is reduced due to its tendency to detach from the body, the "efficacy of

delivery and absorption of the active ingredient is greatly reduced" and can’t fairly be called "maximum strength." Id. ¶ 26. Agee also alleges that the term "Maximum Strength" tells consumers that the patch "contains and delivers the maximum amount of lidocaine available in patch form and is superior, or at least equivalent, in efficacy and results to other OTC and prescription-strength lidocaine patches." Id. ¶ 27. Finally, Agee alleges the language stating that the patch will "Desensitize Aggravated Nerves" and provide "Numbing Relief" "For Back, Neck, Knees, Shoulders & Elbows" "falsely impl[ies] the Product completely blocks and desensitizes nerves and pain receptors, eliminates responses to painful stimuli, and can treat neuropathic and musculoskeletal pain, including back and spinal pain." Id. ¶¶ 29, 30.

Agee alleges that these representations and omissions mislead consumers about the quality of the product. She alleges that at the time of her purchase, she understood the label to represent that the patch "would reliably adhere to her body and deliver a 4% lidocaine dose for 8 hours." Id. ¶ 69. Agee says that she would not have purchased the product or would have paid less for it if she had known that some or all of the label's representations were untrue. Id. ¶¶ 70-72, 74.

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