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Have you ever read the warning label on a bottle of weed killer?
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I can't think of any better way to spend a Saturday reading warning labels.
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Yeah, most people don't. They trust the label.
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They figure if it's on the shelf at the garden store, someone checked it.
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But what happens when a farmer or a homeowner gets cancer?
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And it turns out the label never warned them.
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Who decides whether that warning should have been there?
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A federal agency or a jury?
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That's the question Monsanto desperately wants answered in its favor.
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And it's exactly what we're digging into today in Monsanto versus Dernel.
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You really should do it. You might regret it if you don't.
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Too dark. Questions about this case? Reach out to us via LinkedIn at the High Court report.
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All right, here's what you need to know. The court agreed to decide.
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Whether the federal insecticide, fungicide, and rodenticide act,
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fifra, pre-empts, meaning wipes out, a label-based failure to warn lawsuit
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when EPA approved the label and didn't require the warning.
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Okay, let me translate. Fifra, the federal pesticide law, runs a whole
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registration system. Before any pesticide hits the shelf,
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Monsanto has to submit data to EPA. EPA reviews it, decides the product doesn't pose
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unreasonable risk, and approves the label. The label goes on the bottle and a story, right?
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That's what Monsanto says. End of story.
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Dernel says not so fast, because fifra also has this separate provision that says
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a pesticide becomes illegal to sell the moment it becomes misbranded,
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meaning the label misleads consumers or omits a warning it should carry.
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And here's the kicker. Fifra explicitly says that EPA's decision
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to register a pesticide is not, and I'm quoting the statute,
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a defense for the commission of any offense under federal law.
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Right, so Monsanto says the label EPA approved is the law.
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Dernel says actually courts and juries decide whether that label broke the law.
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That's the fight. Let's back up and tell John Dernel's story.
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He started spraying Roundup in 1996.
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Monsanto's flagship glyphosate-based weed killer.
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He sprayed it for more than 20 years.
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No protective equipment, no cancer warning on the bottle.
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He trusted the label. Monsanto's marketing told him Roundup was safe.
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Then in 2018, he got a diagnosis of mantle cell lymphoma,
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a rare and aggressive blood cancer.
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He sued Monsanto in Missouri State Court,
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and the jury, after hearing the evidence,
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awarded him $1.25 million on his failure to warn claim.
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But here's the thing, the jury rejected every other claim he brought.
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Designed effect? Gone.
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Other statutory claims? Gone.
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Just the failure to warn.
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And to reach that verdict, the jury necessarily found two things.
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Roundup increased Dernel's cancer risk, and Monsanto never told him.
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Monsanto appealed, arguing the claim never should have gotten to a jury.
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Federal law blocked it entirely.
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The Missouri Court of Appeals disagreed and affirmed the verdict.
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The Missouri Supreme Court declined to take the case,
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and now it's at the Supreme Court.
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The Court granted cert because this touches one of the biggest
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unresolved questions in modern preemption law.
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Does a federal agency stamp of approval
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insulate manufacturers from state tort liability?
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There's no clean-circuit consensus,
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and with over 100,000 Roundup lawsuits pending nationally,
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the stakes demanded a definitive answer.
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All right, let's get into the arguments.
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Monsanto goes first.
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Monsanto's first argument,
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when EPA registers a pesticide,
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it makes a product-specific judgment
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that the label contains all warnings necessary to protect human health.
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That judgment constitutes a binding federal requirement.
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And Fiffer's preemption clause says,
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states can't impose labeling requirements
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in addition to or different from those required under the federal law.
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So Monsanto's theory is,
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EPA reviewed decades of cancer data on glyphosate
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and said no cancer warning needed.
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That determination locked in the label.
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A Missouri jury can't then say,
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you needed a cancer warning.
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And Monsanto leans hard on regal versus metronic.
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That's a 2008 Supreme Court case,
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where the court held that FDA's pre-market approval
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of a medical device imposed specific federal requirements
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that preempted state tort claims.
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Monsanto says same thing here.
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EPA's registration is just like FDA's pre-market approval.
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The analogy Monsanto uses,
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EPA is to round up label what FDA is to a pacemaker design.
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When the federal government reviewed it,
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approved it, and said this is what you use,
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states can't demand something different.
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Monsanto's second argument,
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even if you think state failure to warn law
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can sometimes survive preemption,
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because Missouri standard differs from FIFRA's standard.
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Here's the difference they point to.
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FIFRA requires EPA to weigh the economic,
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social, and environmental costs and benefits of pesticide use
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when deciding whether a warning is necessary
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to protect health in the environment.
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Missouri juries get no such instruction.
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Missouri presents unreasonable danger
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to a jury without definition.
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No cost-benefit analysis required.
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And Monsanto says that gap matters.
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A Missouri jury sees an injured plaintiff with cancer
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and never confronts the farmer who depends on roundup to feed the country.
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EPA balance those competing interests.
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Monsanto's third argument, impossibility.
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Even if you think Missouri law can survive express preemption in some cases,
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it can't hear, because Monsanto physically could not do
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what Missouri law demanded.
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Federal law made it unlawful to distribute roundup
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with a label substantially different
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from the EPA-approved version.
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Adding a cancer warning would be substantially different.
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And in 2019, EPA sent a letter to all glyphosate manufacturers.
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Explicitly warning them that a cancer label would render their products
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misbranded, illegal under federal law.
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So Monsanto says, state law told us to add a cancer warning.
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Federal law said, add that warning and you break federal law.
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You can't comply with both.
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And Monsanto draws a direct line to PLEVA vs.
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2011 Supreme Court case on generic drug labels,
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where the court said,
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if you can't independently do under federal law
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what state law requires, it's preempted.
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Now, Dernel fires back.
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And his first response is the biggest one.
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everything Monsanto just argued assumes that EPA's registration decision
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settles whether roundups label violated the misbranding prohibition.
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But Fifre never gave EPA that power.
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Dernel leans on Loperbright Enterprises versus Riemondo,
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a 2024 Supreme Court case that eliminated judicial
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deference to agencies interpreting their own statutes.
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After Loperbright, an agency's reading of a statute
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binds courts only when Congress explicitly
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delegated that interpretive authority.
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find me one sentence in Fifre that delegates to EPA,
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the power to conclusively determine whether a pesticide label
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violates the misbranding prohibition.
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He points straight to Fifre's text,
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in no event shall registration be construed as a defense
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for the commission of any offense under the subchapter.
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The statute literally says EPA's approval
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can't shield manufacturers from a misbranding charge.
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EPA's determination amounts to prima facie evidence,
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a rebuttable presumption, not a final verdict.
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And he stacks the evidence.
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Fifre provides for jury trials and condemnation proceedings
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over misbranded pesticides.
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Fifre provides jury trials in civil penalty cases.
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Fifre authorizes criminal prosecution
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with jury trial rights.
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None of that makes sense if EPA already
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decided the question conclusively.
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Dernel's second argument,
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Missouri law and Fifre say the same thing,
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both forbid selling a pesticide with a misleading
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or inadequate label.
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When state and federal law prohibit identical conduct,
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there's no conflict.
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They run parallel, not in opposition.
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He points to baits versus Dow agro sciences,
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the 2005 Supreme Court case that first drew the lines here,
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which held that state failure to warn law,
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targeting false or misleading pesticide labels,
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is not preempted because it mirrors
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Fifre's misbranding provisions.
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The jury found Roundup's label,
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misleading and inadequate.
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That finding enforces Fifre's own standards.
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And Dernel adds a procedural gut punch.
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Bates put the burden on Monsanto.
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If you think Missouri law reaches beyond Fifre,
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you request a jury instruction telling the jury
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to apply Missouri law consistent with federal standards.
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Monsanto never asked for that instruction,
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never challenge the jury instructions at trial,
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never raise the issue on appeal,
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Dernel's third argument on impossibility.
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Monsanto could have added a cancer warning
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without asking EPA's permission.
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And actually, Monsanto's own parent company proved it.
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In 2012, Bayer Crop Science,
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added a California Proposition 65 cancer warning
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to a different pesticide label,
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through a simple notification procedure to EPA.
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EPA confirmed the change fell
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within permitted notification rules.
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Dernel argues EPA's own regulations from 1995 and 1998
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allowed manufacturers to add advisory statements
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related to precautions by notification.
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No approval required.
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Monsanto sat on its hands.
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It never asked EPA to approve a cancer warning.
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Under the all-brecht standard from 2019,
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you can't claim impossibility if you never tried.
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And Dernel's fallback,
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even if Monsanto genuinely could not change the label,
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Fifre still required it to stop selling a pesticide
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the jury found misbranded.
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Both state and federal law demand the same response.
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When both sovereigns command cessation,
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cessation is both possible and required.
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So what does this actually mean for real people?
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If Monsanto wins and the court rules Fifre pre-empts
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failure to warn claims when EPA approved the label
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over 100,000 roundup lawsuits effectively collapse,
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that $7.25 billion class settlement buyer announced,
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the remaining nearly $1 billion in pending appeals,
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the opt out cases gone,
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or dramatically reduced in value,
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and the implications reach beyond roundup.
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Every manufacturer of an EPA registered pesticide gains a shield.
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Get the EPA label approved,
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and state-tort law can't touch you,
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no matter what juries might think about whether
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your label warned consumers adequately.
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On the flip side, if Dernel wins,
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pesticide manufacturers face liability in every state court,
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with every jury applying its own version of what
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adequate warning means.
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Monsanto warns that means a patchwork of conflicting verdicts,
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overwarning that waters down the label's consumers
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actually need to read,
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and reduced incentives to develop next-generation pesticides.
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The agricultural stakes are real.
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President Trump signed an executive order in February,
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2026, declaring that loss of access to glyphosate-based
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herbicides would cause a debilitating impact
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on domestic agricultural capabilities.
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Farmers planted glyphosate-resistant crops
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over a massive share of American crop land.
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No direct replacement exists at scale.
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that's a policy argument for Congress, not this court.
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Any points out that Monsanto actually lobbied Congress
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to add explicit immunity language to FIFRA.
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Blocking state-law liability for labels EPA approved.
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Congress never passed it.
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The fact that Monsanto asked Congress for something,
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the company now claims FIFRA already provides,
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tells you everything.
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So those are the stakes.
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What should we watch for at oral arguments?
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I'd watch for this Loper-bright question front and center.
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Does FIFRA actually delegate to EPA,
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the authority to make binding conclusive pronouncements
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on whether a pesticide label violates the misbranding prohibition?
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If the answer is no,
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Monsanto's entire express preemption theory collapses.
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Expect the justices to press Monsanto hard
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on where in the text that delegation appears.
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And watch for questions about the buyer-larven label change.
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If buyer actually added a cancer warning
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to a pesticide label in 2012 through notification and EPA signed off,
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how does Monsanto claim it faced legal impossibility
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in adding a cancer warning to round up?
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The fault line on the court might run between
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Justice's skeptical of agency power after Loper-bright.
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Who may side with Dernel on the delegation question?
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And Justice's worried about the broader consequences
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of exposing federal agency decisions to jury,
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second-guessing in 50 states.
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And watch for questions about what happens to bates.
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Monsanto's reading of Fifra would arguably require
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a finding of preemption in bates itself,
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because Dow's strong arm label also got EPA registration.
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The court obviously didn't preempt in bates.
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Someone will ask Monsanto to square that circle.
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Why does this case matter?
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Because it draws the line between two visions
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of how federal regulation works.
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In Monsanto's vision, EPA approval means the science question is closed.
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Juries don't reexamine what the government already decided.
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In Dernel's vision, federal registration gives you the right to sell your product,
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but it doesn't immunize you from a jury's finding that your label lied.
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100,000 cancer patients are watching.
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American farmers are watching,
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and every product liability lawyer in the country is watching.
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If you made it this far,
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share this episode with one person who uses round up on their lawn
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and has no idea this case exists, because it might.
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You can find us on Apple Podcasts, Spotify, YouTube,
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just search the High Court report.
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And honestly, subscribing takes less time than reading a pesticide label.
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Hit us up on LinkedIn at the High Court report.