John D. Carson v. Monsanto Company

72 F.4th 1261
Court of Appeals for the Eleventh Circuit·Decided July 10, 2023·No. 21-10994·Published·Cited by 6 cases

Opinion

[PUBLISH]

In the

United States Court of Appeals For the Eleventh Circuit

No. 21-10994

JOHN D. CARSON, Plaintiff-Appellant,

versus MONSANTO COMPANY,

Defendant-Appellee.

Appeal from the United States District Court for the Southern District of Georgia D.C. Docket No. 4:17-cv-00237-RSB-CLR

USCA11 Case: 21-10994 Document: 163-1 Date Filed: 07/10/2023 Page: 2 of 22

2 Opinion of the Court 21-10994

Before WILLIAM PRYOR, Chief Judge, and WILSON, JORDAN, ROSENBAUM, NEWSOM, BRANCH, GRANT, LUCK, LAGOA, BRASHER, ABUDU, and TJOFLAT, ∗ Circuit Judges. WILLIAM PRYOR, Chief Judge, delivered the opinion of the Court, in which JORDAN, ROSENBAUM, NEWSOM, BRANCH, GRANT, LUCK, LAGOA, BRASHER, ABUDU, and TJOFLAT, Circuit Judges, join. JORDAN, Circuit Judge, filed a concurring opinion. WILSON, Circuit Judge, filed a dissenting opinion. WILLIAM PRYOR, Chief Judge:

This appeal presents the question whether, under an express-

preemption provision, a federal agency action that otherwise lacks the force of law preempts the requirements of state law. John Carson developed cancer after decades of using the popular weedkiller Roundup. He sued its manufacturer, Monsanto Company, for failing to warn him that the product can increase users’ cancer risks. The district court ruled that a provision of the Federal Insecticide, Fungicide, and Rodenticide Act, 7 U.S.C. § 136v(b), expressly preempts some of Carson’s claims under Georgia law because the Environmental Protection Agency had approved a label for Roundup that lacked a cancer warning and the Agency classifies Roundup’s main ingredient—glyphosate—as “not likely to be carcinogenic .” Carson argues that his suit is not preempted because the relevant agency actions did not have the force of law, which he

∗ Senior Circuit Judge Tjoflat elected to participate in this decision, pursuant to 28 U.S.C. § 46(c). Judge Jill Pryor is recused.

21-10994 Opinion of the Court 3

characterizes as a prerequisite for express preemption. After a panel of this Court reversed the district court, we granted rehearing en banc to address whether a “force-of-law” analysis is relevant in this context. We conclude that this question must be answered by recourse to ordinary principles of statutory interpretation, and we remand this appeal to the panel to decide whether Carson’s suit is preempted.

I. BACKGROUND

John Carson used Roundup on his lawn for thirty years until 2016, when he was diagnosed with malignant fibrous histiocytoma, a form of cancer. He sued Monsanto, Roundup’s manufacturer, in the district court. He alleged that Monsanto knew or should have known that Roundup was carcinogenic but did not warn users of that danger. See Greenway v. Peabody Int’l Corp., 294 S.E.2d 541, 545– 46 (Ga. Ct. App. 1982) (establishing that a manufacturer must “exercise reasonable care to inform [buyers] of its [product’s] dangerous condition or of the facts which make it likely to be dangerous” (citation omitted)).

Monsanto moved for a judgment on the pleadings on the ground that a provision of the Federal Insecticide, Fungicide, and Rodenticide Act, 7 U.S.C. § 136v(b), expressly preempted Carson’s suit and, in the alternative, that the suit was impliedly preempted by the Environmental Protection Agency’s previous approval of Roundup’s labeling and continued adherence to the reasoning for that decision. The Act expressly preempts a state-law pesticide rule, including a common-law cause of action, if it is a “requirement[]

4 Opinion of the Court 21-10994

for labeling or packaging in addition to or different from those required under” the Act. Id.; see Bates v. Dow Agrosciences LLC, 544 U.S. 431, 443–44 (2005). Monsanto argued that because the Environmental Protection Agency, which administers the Act, had declined to require a cancer warning when it registered and continued to approve Roundup for sale, see 7 U.S.C. § 136a(a), a Georgia-law requirement of a cancer label would be “in addition to or different from” what the Act required.

The district court agreed with Monsanto and granted judgment on the pleadings in Monsanto’s favor insofar as Carson’s suit relied on the lack of a cancer warning in Roundup’s label. Carson v. Monsanto Co., 508 F. Supp. 3d 1369 (S.D. Ga. 2020). The district court assumed in Carson’s favor that Monsanto failed to perform its duty under Georgia law “to provide adequate warnings or other clinically relevant information and data regarding . . . the [cancer] risks associated with” Roundup. Id. at 1376. But it ruled that this state-law requirement was expressly preempted because the Georgia requirement “would be in direct conflict with the EPA’s approved label because the EPA classifies [Roundup’s active ingredient ,] glyphosate[,] as ‘not likely to be carcinogenic to humans’ and considers glyphosate products with cancer warnings to be ‘misbranded .’” Id. The parties reached a partial settlement, and Carson amended his complaint to abandon the claims that were not dismissed .

A panel of this Court reversed. Carson v. Monsanto Co., 51 F.4th 1358 (11th Cir.), reh’g en banc granted, op. vacated, No. 21-10994,

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2022 WL 17813843 (11th Cir. Dec. 19, 2022). It determined that Georgia’s common-law standard for product-safety warnings was less demanding than the federal prohibition against marketing “misbranded” pesticides. Id. at 1363 (citing 7 U.S.C. § 136(q)(1)(G); Greenway, 294 S.E.2d at 545–46). And it held that the Agency’s approval of Roundup labels without a cancer warning, even in the light of the Agency’s internal scientific conclusions about Roundup’s active ingredient, did not preempt the Georgia cause of action. Id. at 1363–65. The panel explained that because “only federal action with the force of law has the capacity to preempt state law[,] . . . any preemption analysis of agency action in the [Federal Insecticide, Fungicide, and Rodenticide Act] context beyond the statute itself first requires us to do a Mead analysis.” Id. at 1362. By “Mead analysis,” the panel referred to the question whether “the agency [is] able to speak with the force of law when it addresses ambiguity in the statute [it administers] or fills a space in the enacted law.” United States v. Mead Corp., 533 U.S. 218, 229 (2001). Because “the EPA registration process” does not have the force of law under the Mead framework, the panel reasoned, the result of that process could not preempt Carson’s suit. Carson, 51 F.4th at 1363– 64. The panel also rejected Monsanto’s implied-preemption theory. Id. at 1364 n.11.

We granted Monsanto’s petition for rehearing en banc and vacated the panel opinion. Carson, 2022 WL 17813843. We instructed the parties to address two questions about how a “force- of-law” analysis applies:

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1. Can an express-preemption provision like § 136v(b) give preemptive effect to a federal agency action that otherwise lacks the “force of law”? Or must a reviewing court determine, as a threshold matter, whether federal agency action has the “force of law”? 2. How should a reviewing court identify the federal “requirements . . . under this subchapter” to which § 136v(b) refers, and what role, if any, does a “force of law” analysis play in that determination?

II. JURISDICTION

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