Written: July 30, 2025 – 14:00 EDT

U.S. health regulators are seeking to curb the growing use of a potent kratom-derived chemical increasingly found in gas station supplements, citing concerns over public health and its opioid-like effects. The move comes after pressure from both within the supplement industry and public health advocates calling for tighter oversight.

What is 7-hydroxymitragynine and why is it under scrutiny?

The substance at the center of the U.S. Food and Drug Administration’s (FDA) latest crackdown is 7-hydroxymitragynine (7-OH), a powerful compound derived from Mitragyna speciosa, commonly known as kratom. Native to Southeast Asia, kratom has traditionally been used in small doses as a stimulant or pain reliever. However, in the U.S., it has gained popularity in recent years as an unapproved remedy for conditions such as chronic pain, anxiety, and opioid withdrawal.

Unlike the natural kratom leaf, 7-OH is a concentrated and often synthetically enhanced form of the plant’s active compounds. The FDA warns that the chemical behaves like an opioid and, in some cases, may be stronger than morphine.

“7-OH is an opioid that can be more potent than morphine,” said FDA Commissioner Dr. Marty Makary in a statement. “We need regulation and public education to prevent another wave of the opioid epidemic.”

FDA recommends federal ban; DEA to decide next steps

In a report released on Tuesday, the FDA called for placing 7-OH on Schedule I of the Controlled Substances Act—the same category as heroin, LSD, and ecstasy. Schedule I is reserved for substances deemed to have no currently accepted medical use and a high potential for abuse.

The recommendation now heads to the Drug Enforcement Administration (DEA), which holds the authority to schedule or ban substances at the federal level. A national ban would require formal rulemaking, including public commentary and interagency review.

Importantly, the FDA emphasized that the action does not target natural kratom leaves, which are still legally available in many parts of the U.S., though not without controversy.

“This move is focused specifically on synthetic and highly concentrated derivatives like 7-OH,” the U.S. Department of Health and Human Services (HHS) clarified in its statement.

Growing use in convenience-store products raises alarms

7-OH is frequently found in over-the-counter supplements, including energy drinks, gummies, powders, and capsules marketed in gas stations and convenience stores. These products often lack FDA approval, are not evaluated for safety, and in some cases make unverified medical claims, such as treating arthritis, anxiety, or opioid withdrawal.

In June, the FDA issued warning letters to seven companies marketing such products, citing violations of federal rules. Regulators highlighted the health risks associated with the ingredient and flagged the lack of clinical data supporting its safety.

The FDA’s action follows increasing complaints from the dietary supplement industry itself. Some kratom sellers argue that synthetic or purified 7-OH poses a danger to consumers and undermines the credibility of the broader market.

Industry split: Regulation welcomed by some, opposed by others

Ryan Niddel, CEO of Diversified Botanics, a Utah-based kratom supplement company, praised the FDA’s move.

“The FDA demonstrated the exact kind of data-driven, proactive regulatory excellence needed to safeguard unwitting consumers across the U.S.,” Niddel said.

However, the issue has caused a rift within the kratom industry.

The American Kratom Association (AKA), a prominent lobbying group, has long advocated to keep kratom unregulated, pushing for legislation that would prevent the FDA from applying stricter rules than those used for standard food and supplements.

On the other hand, the Holistic Alternative Recovery Trust (HART), which supports access to 7-OH-based therapies, criticized the FDA’s move, suggesting it was influenced by market-driven motives.

“Big kratom trade groups have spent years blaming 7-OH for harms caused by their own unregulated products, because it threatens their market share,” the organization stated via email.

A history of federal resistance to kratom regulation

This is not the first time U.S. authorities have considered a ban on kratom or its derivatives. In 2016, the DEA proposed classifying kratom as a Schedule I drug, triggering widespread backlash. Public opposition, including a letter signed by more than 60 members of Congress, ultimately halted the ban.

Following the failed attempt, the FDA initiated a deeper investigation into kratom’s pharmacological effects. In 2018, the agency concluded that the plant contains multiple opioid-like compounds, supporting its potential for abuse and risk of addiction.

Since then, the FDA has continued to warn consumers about injuries, overdoses, and deaths linked to kratom supplements. These products, often sold in capsule or powder form, are widely accessible both online and in retail outlets, despite lacking FDA approval.

Broader crackdown on unapproved substances sold as supplements

The FDA’s actions against 7-OH are part of a wider campaign targeting unregulated substances sold under the guise of dietary supplements or energy boosters. In recent months, regulators have also issued warnings against products containing tianeptine, a substance sometimes called “gas station heroin.” Although banned in several states, tianeptine remains unregulated at the federal level.

By moving to ban 7-OH, health officials are aiming to get ahead of potential public health risks before they escalate further.

What happens next?

The DEA’s review process could take several months, involving public comment periods and scientific evaluation. In the meantime, the FDA continues to monitor the market and issue warnings to manufacturers selling unapproved or unsafe products.

Consumers are advised to check labels, avoid products claiming to treat medical conditions without FDA approval, and consult health professionals before using supplements containing kratom or its derivatives.

Final thoughts

As the U.S. continues to grapple with the long-lasting effects of the opioid epidemic, federal health officials appear determined to close regulatory loopholes and limit public exposure to potent, opioid-like compounds such as 7-OH. While natural kratom use remains contentious, the synthetic version’s potential for abuse and misuse has drawn sharp attention from regulators and public health advocates alike.

Source: AP News – US health officials crack down on kratom-related products after complaints from supplement industry

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If you recently bought tomatoes in Georgia, North Carolina, or South Carolina, it’s time to check your kitchen. A serious recall is now underway, and the FDA has labeled it the most urgent kind—Class I—meaning the contaminated product could lead to severe illness or even death.

What’s Going On?

The recall was first issued on May 2, but things have since escalated. The tomatoes in question may be contaminated with salmonella, a bacteria that can cause serious health complications—especially in vulnerable groups like young children, the elderly, pregnant women, and those with weakened immune systems.

The tomatoes were distributed by Williams Farms Repack LLC, based in Lodge, South Carolina, and sold to wholesalers and distributors under the H&C Farms Label between April 23 and April 28.

Where Were the Tomatoes Sold?

The recalled tomatoes ended up in:

• Georgia
• North Carolina
• South Carolina

What Tomato Sizes and Lots Are Affected?

Here’s what to look for on packaging labels:

• 5×6; Lot Code: R4467
• 6×6; Lot Codes: R4467, R4470
• Combo, 25-pound box; R4467
• 4×4, 2-layer; R4467
• 4×5, 2-layer; R4467
• 60-count, 2-layer; R4467
• 60-count, 18 pounds loose; R4467, R4470
• XL, 18 pounds loose; R4467
• 3-count trays; R4467

Why This Is Serious: Understanding Salmonella

Salmonella isn’t something to take lightly. According to the CDC, symptoms usually begin 12 to 72 hours after eating contaminated food and may include:

• Diarrhea
• Fever
• Abdominal cramps

While many people recover without treatment, in some cases—particularly among vulnerable populations—the infection can lead to hospitalization and life-threatening complications.

Worryingly, freezing or drying the tomatoes won’t kill the bacteria. Salmonella can survive for weeks in dry environments and months in moist ones.

So Far, No Reported Illnesses—But Stay Cautious

As of the FDA’s latest update on May 28, no illnesses or deaths have been reported. Still, the agency isn’t taking any chances.

Bought These Tomatoes? Here’s What To Do

The FDA is urging consumers:

• Don’t eat the recalled tomatoes.
• Return them to the place of purchase for a full refund, or safely discard them.
• Feeling sick after eating them? Contact your healthcare provider right away.

Stay safe, stay informed—and always double-check your produce when recalls are announced. For ongoing updates, visit the FDA’s recall website.

Source: USA Today – Tomatoes sold in 3 states now labeled deadly by FDA

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Coffee lovers, it’s time to double-check your morning brew! On March 25, the Food and Drug Administration (FDA) issued a Class II recall for certain coffee products from Massimo Zanetti Beverage USA. The recall affects coffee sold under the “Our Family” brand, and it’s all due to a mislabeling issue.

The recall was triggered after a portion of Our Family Traverse City Cherry-Flavored Decaf Light Roast Ground Coffee was mislabelled as decaffeinated. The product, which comes in 12-ounce bags with a best-buy date of August 8, 2025, had the wrong label, causing confusion about its caffeine content.

Massimo Zanetti Beverage USA, the company behind the coffee, voluntarily initiated the recall on March 13. As of now, the recall remains active, and the company has yet to provide a resolution.

This recall is classified as a Class II risk by the FDA. While the product may cause temporary or medically reversible health consequences if consumed, the chances of serious harm are minimal. However, for individuals who are sensitive to caffeine or need to avoid it for health reasons, it’s best to return or dispose of the product.

The recall affects 692 cases of the mislabeled coffee, which were distributed across 15 states:

• Colorado
• Iowa
• Illinois
• Indiana
• Kansas
• Kentucky
• Mississippi
• Minnesota
• North Carolina
• North Dakota
• Nebraska
• Ohio
• South Dakota
• Wisconsin
• Wyoming

If you have purchased this product in any of these states, be sure to check the packaging to see if your coffee is part of the recall.

If you have a bag of the affected coffee, you should stop using it immediately. You can return it to the store for a refund or dispose of it according to the FDA’s guidelines.

The company, Massimo Zanetti Beverage USA, has yet to comment on the recall request from PEOPLE.

This is not the only coffee-related recall this year. Earlier this month, the FDA issued a recall for over 75,000 bottles of two International Delight Coffee Creamers. The recall followed complaints of spoilage and illness linked to a texture issue in the creamers, though no food safety concerns were reported. Like the coffee recall, this was also classified as a Class II risk.

Danone, LLC, the parent company of International Delight, stated that the spoilage issue was caused by premature product deterioration and emphasized that the risk to consumers was minimal. Still, they opted for a voluntary recall to address the quality concern.

It’s been a year of recalls, with several food and beverage products affected, including:

• Dark chocolate products from Cal Yee Farms
• Baked goods from one of Dunkin’s vendors
• Cheese from Aldi
• Coca-Cola soda packs

These recalls highlight the ongoing effort by companies and the FDA to ensure consumer safety, even when risks are low.

While this recall is mostly about a mislabeling error, it’s a good reminder to always stay up to date on food recalls, especially if you’re sensitive to certain ingredients or caffeine. If you’re in one of the affected states and have purchased the recalled coffee, make sure to check the label and take action if necessary.

In the meantime, coffee lovers can breathe easy knowing that while this may be an inconvenience, the risk to health is low. Keep an eye out for more recall updates as the year progresses.

Source: People – FDA Issues Recall for Coffee Grounds in 15 States

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