August 16, 2021
The Petition underscores that consistent regulatory assessments in the U.S. and worldwide, and the overwhelming weight of scientific evidence, support the conclusion that glyphosate-based herbicides are safe and not carcinogenic. In light of the Environmental Protection Agency’s approval of the Roundup label without a cancer warning, any state-law failure-to-warn claims premised on such warning would conflict with federal law and thus are preempted.
Courts across the U.S. have divided on this basic question of when federal law preempts state law, which makes review by the U.S. Supreme Court both important and necessary. It has been 16 years since the Supreme Court ruled on Federal Insecticide, Fungicide and Rodenticide Act preemption, and the prior case did not involve a warning that EPA had rejected.
Earlier this year, Bayer announced a five-point plan to manage and resolve future litigation risk arising from the Roundup litigation. Supreme Court review and reversal of the Ninth Circuit’s flawed ruling is a major factor in this plan and likely will determine whether the litigation will largely end (if the court issues a favorable decision on a cross-cutting issue like federal preemption) or the company implements a claims process to resolve claims over the next 15 years (in the event of an adverse outcome).
Bayer took an additional provision in Q2 2021 to reasonably account for future litigation exposure in the event of an adverse outcome. Bayer expects the Supreme Court to decide in the next six months whether it will grant review of the Hardeman case.
On federal preemption, Bayer argues that state-law failure-to-warn claims should be preempted on the grounds of both express preemption, because they are preempted by a specific statutory provision, and conflict preemption, because the state-law claims necessarily conflict with federal requirements.
On express preemption, the Petition argues the Ninth Circuit erred by holding that the state-law claims were not “in addition to or different” from FIFRA’s requirements, even though they conflicted with the EPA’s consistent finding that glyphosate does not cause cancer in humans. This result is compelled by Supreme Court precedent, which the Petition explains, holds that “where EPA determines that a pesticide should be accompanied by one warning (such as ‘CAUTION’) but a jury concludes under state law that the label should include a more aggressive one (such as ‘DANGER’), state law is preempted.” The Ninth Circuit’s reading of the “in addition to or different” language also splits with how other courts have understood similar preemption provisions in other federal statutes.
On conflict preemption, the Ninth Circuit wrongly held that there was no conflict between the state-law claims and FIFRA’s requirements, even though EPA would not approve the kind of label required by the state-law jury verdict and even though Monsanto cannot unilaterally change its label without agency approval. This ruling also conflicts with Supreme Court precedent, which holds that either scenario establishes implied preemption.
If left in place, the Ninth Circuit’s ruling would lead to a highly undesirable result. States could require pesticide manufacturers to include warnings on their labels, even when EPA has expressly informed manufacturers that doing so would be unlawful.
With regard to expert evidence, the Petition explains that the Ninth Circuit wrongly blessed the admission of expert testimony on the issue of whether glyphosate caused Mr. Hardeman’s cancer even though that testimony “rested on little more than subjective intuitions.” This result conflicts with Federal Rule of Evidence 702 and Supreme Court precedent, which require “trial courts to play ‘a gatekeeping role’ to ensure that expert opinions are reliable … [and] the product of ‘reliable principles and methods,’ ‘reliably applied … to the facts of the case.’”
The Petition states that the Ninth Circuit’s lenient standard “has distorted [existing law] beyond recognition,” and “blurs the boundaries between science and speculation with a third category called ‘art,’” or unsupported intuitions purportedly rooted in clinical experience. The brief argues that “no matter how much clinical experience an expert has, intuition without scientific validation is not ‘the product of reliable principles and methods.’” The argument concludes: “By requiring trial courts to admit expert conclusions that are based on clinical experience – even when sound scientific evidence refutes those conclusions – the Ninth Circuit has codified the fallacy that when scientists speak, their views are necessarily rooted in reliable scientific principles.”
This release may contain forward-looking statements based on current assumptions and forecasts made by Bayer management. Various known and unknown risks, uncertainties and other factors could lead to material differences between the actual future results, financial situation, development or performance of the company and the estimates given here. These factors include those discussed in Bayer’s public reports which are available on the Bayer website at www.bayer.com. The company assumes no liability whatsoever to update these forward-looking statements or to conform them to future events or developments.
Source: Bayer, which is solely responsible for the information provided and is wholly owned by the source. Informa Business Media and all its subsidiaries are not responsible for any of the content contained in this information asset.
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