Christine Vitello v. Natrol, LLC

50 F.4th 689
CourtCourt of Appeals for the Eighth Circuit
DecidedOctober 6, 2022
Docket21-3150
StatusPublished
Cited by20 cases

This text of 50 F.4th 689 (Christine Vitello v. Natrol, LLC) is published on Counsel Stack Legal Research, covering Court of Appeals for the Eighth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Christine Vitello v. Natrol, LLC, 50 F.4th 689 (8th Cir. 2022).

Opinion

United States Court of Appeals For the Eighth Circuit ___________________________

No. 21-3150 ___________________________

Christine Vitello, on behalf of herself and others similarly situated

lllllllllllllllllllllPlaintiff - Appellant

v.

Natrol, LLC

lllllllllllllllllllllDefendant - Appellee ____________

Appeal from United States District Court for the Eastern District of Missouri - St. Louis ____________

Submitted: June 15, 2022 Filed: October 6, 2022 ____________

Before LOKEN and KELLY, Circuit Judges, and MENENDEZ, District Judge.* ____________

LOKEN, Circuit Judge.

The Missouri Merchandising Practices Act (“MMPA”) declares unlawful the use “of any deception, fraud, false pretense, false promise, misrepresentation, unfair practice or the concealment, suppression, or omission of any material fact in

* The Honorable Katherine M. Menendez, United States District Judge for the District of Minnesota, sitting by designation. connection with the sale . . . of any merchandise in trade or commerce.” Mo. Rev. Stat. § 407.020.1. The MMPA authorizes a private damage action by any consumer who “purchases or leases merchandise . . . and thereby suffers an ascertainable loss of money or property . . . as a result of the use . . . by another person of a method, act or practice declared unlawful.” § 407.025.1. The primary issue on this appeal is whether a pharmaceutical purchaser suffers an ascertainable loss caused by the seller’s misrepresentation of supporting clinical studies when the product’s packaging states that it does not provide the benefit the purchaser is seeking. The district court answered this question in the negative and, based on Christine Vitello’s discovery admissions, granted Natrol, LLC’s motion for summary judgment dismissing Vitello’s MMPA and unjust enrichment claims. Vitello appeals. Reviewing the grant of summary judgment de novo, we affirm. See Toben v. Bridgestone Retail Operations, LLC, 751 F.3d 888, 896 (8th Cir. 2014) (standard of review).

I. Background

A. The Transactions at Issue. Vitello was diagnosed with attention-deficit disorder (“ADD”) in 2004 and was prescribed Adderall to treat symptoms that included “[b]eing forgetful, disorganized, scatterbrained” and “[n]ot being able to retain anything.” Apart from isolated pauses to avoid negative side effects, Vitello used Adderall as prescribed for thirteen years, noticing a “pretty significant difference in memory and concentration.”

On June 22, 2017, Vitello saw Cognium, a “nutraceutical” manufactured by Natrol, on sale in Arnold, Missouri. Cognium, according to Natrol’s advertising, improves memory and concentration. Its packaging stated that Cognium is “powered by Cera-Q, a natural protein from silkworm cocoons,” and can improve “Memory Recall Efficiency” by 90% when taken twice daily for four weeks. The box claimed that “[n]ine clinical studies in adults, seniors and children showed statistically significant improvements in memory and cognition in 4 weeks or less when taken as

-2- directed.” The Cognium bottle also contained two disclaimers that frame the issue on appeal: first, below “Clinically Proven to Improve Memory and Concentration” statements, an FDA-mandated disclaimer for all nutritional supplements:

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

See 21 C.F.R. § 101.93(c)(2). Second, at the end of the “Supplement Facts” statements: “Consult your healthcare professional prior to use if you have or suspect a medical condition, are taking prescription drugs, or if you are pregnant or lactating.”

After reading the packaging, Vitello purchased a box of Cognium for $19.97. Without consulting her doctor, Vitello quit Adderall “cold turkey” and started taking Cognium five to seven days later. She took Cognium twice daily for sixty days, purchasing a second bottle on July 31 for $16.97. She noticed no positive effect in memory or concentration, feeling “almost exactly the same on Cognium as before I was on Adderall.”

In June 2018, Vitello filed a putative class action complaint against Natrol, seeking damages for herself and establishment of a National Class and Missouri Consumer Subclass. Vitello alleged that, prior to her purchases of Cognium, two of the nine clinical studies noted on its packaging had been retracted, including one for “data fabrication and falsification”; that Natrol did not update its packaging or inform consumers of the retractions; and that Vitello “would not have purchased the Cognium and sustained the loss had [Natrol] disclosed in its box/packaging, bottle, and brochure that two (2) of the nine (9) clinical studies had been retracted for data manipulation and fraud/fabrication.” She asserted causes of action for violations of the MMPA and unjust enrichment. After suit was filed, consistent with its advertised

-3- money back guarantee, Natrol issued a refund check to Vitello for the purchase price of the two bottles of Cognium she bought. Vitello refused to cash the check.

B. Procedural History. In December 2018, the district court1 denied Natrol’s Rule 12(b)(6) motion to dismiss the Class Action Complaint for failure to state a claim, concluding that Vitello alleged sufficient facts to support the elements of her MMPA and unjust enrichment damage claims. The court issued a case management order directing that discovery first proceed on class certification issues. After discovery including interrogatories, document production, and depositions of Vitello and a Natrol representative, Vitello moved for class certification. Natrol opposed and moved for summary judgment dismissing Vitello’s individual claims, submitting in support a Statement of Uncontroverted Material Facts. Rather than respond to the Statement, Vitello filed a motion seeking additional discovery from two Natrol potential expert witnesses. See Fed. R. Civ. P. 56(d).

After considering both parties’ motions and reviewing the completed discovery, the district court2 concluded that one of Natrol’s summary judgment arguments posed a purely legal question -- whether Vitello’s admissions at her deposition that she took Cognium as a substitute for Adderall without consulting her doctor precluded her from proving an MMPA or unjust enrichment claim. The court denied Vitello’s Rule 56(d) motion because it sought additional discovery not relevant to this issue of law and ordered her to respond to Natrol’s summary judgment motion. After Vitello did so, the court found her brief largely unresponsive. The court granted summary judgment for Natrol on both the MMPA and unjust enrichment claims, concluding that Vitello’s admissions that she purchased Cognium

1 The Honorable Rodney W. Sippel, United States District Judge for the Eastern District of Missouri. 2 The Honorable Sarah E. Pitlyk, United States District Judge for the Eastern District of Missouri, to whom the case had been reassigned.

-4- as a substitute for the Adderall prescribed to treat her ADD, without consulting her physician, was direct non-compliance with the disclaimers printed on the Cognium packaging that precluded her from proving her MMPA and unjust enrichment claims as a matter of law. With Vitello’s individual claims dismissed, the court determined the sole named plaintiff could not represent the purported class and dismissed the entire action. See In re Milk Prod.

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Bluebook (online)
50 F.4th 689, Counsel Stack Legal Research, https://law.counselstack.com/opinion/christine-vitello-v-natrol-llc-ca8-2022.