Texas AG Sues Kratom Retailers for Violating State Law Limits
Texas Attorney General Ken Paxton has filed lawsuits against retailers for selling kratom products that allegedly exceed state potency limits.
⚠ "Cat's Claw" Product Warning
New brands falsely marketed as containing Cat's Claw (Rhynchophylline) — a plant that is NOT psychoactive — may actually contain MGM-15, MGM-16, or undisclosed synthetic pharmaceutical compounds that do not appear on standard drug tests. Consumers may be unknowingly ingesting dangerous experimental substances.
News, health information, and legal updates regarding kratom lawsuits and 7-OH class actions.
Texas Attorney General Ken Paxton has filed lawsuits against retailers for selling kratom products that allegedly exceed state potency limits.
The FDA is taking steps to restrict novel potent opioid products, including 7-OH, through seizures and warning letters to marketing firms.
Missouri AG Catherine Hanaway is suing a kratom manufacturer, alleging the sale of MGM-15, a compound claimed to be more potent than 7-OH.
The DEA issued notices of intent to temporarily control 7-hydroxymitragynine (7-OH) and related synthetic derivatives like MGM-15 due to high abuse potential.
The U.S. Drug Enforcement Administration has designated three 7-hydroxymitragynine-related compounds—mitragynine pseudoindoxyl, MGM-15, and MGM-16—as Schedule I substances.
Users of three synthetic opioids -- mitragynine pseudoindoxyl (MP), MGM-15, and MGM-16 -- will be unable to buy products containing them legally as of August 26, 2026.
Mitragynine pseudoindoxyl, MGM-15 and MGM-16 are being temporarily placed in Schedule I as federal officials target manufactured opioid products.
The FDA took action against companies marketing 7-hydroxymitragynine products to protect consumers.
Ohio state regulators issued an emergency rule to classify 7-OH and related substances as controlled substances.
The AMA has adopted a policy urging the FDA to ban the sale and marketing of 7-hydroxymitragynine products.
Missouri AG Catherine Hanaway filed a lawsuit against EDP Kratom, citing the dangers of the potent compound MGM-15.
The DEA filed a Notice of Intent to temporarily place 7-OH above a specific threshold into Schedule I.
The DEA has officially placed three synthetic kratom derivatives into Schedule I, effective August 26, 2026.
Attorney General Ken Paxton filed suit against retailers for allegedly selling kratom products that exceed state limits on alkaloid concentrations.
The American Medical Association has adopted a policy urging the FDA to ban the sale, distribution, and marketing of products containing the kratom alkaloid 7-OH.
A Missouri-based kratom company destroyed millions of dollars worth of inventory following federal regulators' decision to place kratom-related opioids in Schedule I.
The U.S. Drug Enforcement Administration filed its intent to temporarily place 7-hydroxymitagynine (7-OH) and three related substances, including MGM-15, into Schedule I of the Controlled Substances Act.
The Global Kratom Coalition supports the DEA's decision to schedule synthetic alkaloids while protecting access to natural kratom leaf.
The DEA is moving to ban concentrated forms of the kratom alkaloid 7-hydroxymitragynine, classifying it as a Schedule I substance.
The DEA has finalized emergency scheduling for synthetic kratom derivatives, making possession of products containing MGM-15 or MGM-16 a federal offense.