This is not a formal product recall. It’s a public health warning, and the distinction matters. The FDA is telling consumers directly to stop using these products while its investigation continues, rather than issuing a traditional recall notice for each one.

Here’s what you need to know, in plain terms: what the warning covers, why yellow oleander is dangerous, how to check whether your supplement is on the list, and what to do next.

What This Warning Covers

Tejocote root is marketed as a natural weight-loss aid. You may have seen it sold under names referencing “Raiz de Tejocote,” “Crataegus mexicana,” or “Mexican Hawthorn.” It’s popular in weight-loss supplement circles and is often marketed to Spanish-speaking consumers, sold online and in some retail and botanica settings nationwide.

The problem isn’t the marketing claims. It’s what’s actually inside the capsule or bottle. FDA testing has found that a growing list of these products, 33 as of the September 17, 2026 update, are contaminated or substituted with yellow oleander (Thevetia peruviana), a completely different and poisonous plant that closely resembles tejocote root.

Two newly named products in this update are “D Magic Plus” and “B. Magi.” The FDA also identified two products in the broader list that contained undisclosed drug ingredients on top of the yellow oleander contamination.

This isn’t a one-time finding. The FDA’s investigation traces back to a 2023 CDC report that first documented yellow oleander substitution in tejocote root products. Since then, the agency has continued testing more products and expanding its warning list as new contamination turns up.

Why It’s Dangerous

Yellow oleander is not a mild substitution. It contains cardiac glycosides, compounds similar to those found in the heart medication digoxin.

In a controlled medical dose, compounds like this can be therapeutic. Consumed unknowingly in an unregulated supplement, they’re a different story entirely.

The FDA states that yellow oleander can cause neurologic, gastrointestinal, and cardiovascular effects that may be “severe, or even fatal.” The cardiovascular risk, specifically dangerous heart rhythm changes, is the most serious concern.

This particular September 17, 2026 update does not cite specific illnesses or deaths tied to this round of findings. That doesn’t make the risk any less real: it’s exactly why the FDA continues to expand and update this warning as it tests more products.

How to Check Your Supplement

You cannot tell whether your supplement is contaminated just by looking at it. The label will still say tejocote root. It won’t say yellow oleander.

That’s what makes this warning worth taking seriously even if your particular bottle isn’t one of the two newly named products. Here’s how to check:

• Look at your supplement label for any reference to tejocote root, Raiz de Tejocote, Crataegus mexicana, or Mexican Hawthorn.
• Check specifically for “D Magic Plus” or “B. Magi,” the two products newly named in this September 17, 2026 update.
• Visit the FDA’s official warning page (linked below) for the current, full list of affected products and brand names, since the FDA has been adding to this list over time.
• If you’re unsure whether your specific product matches something on the list, treat it as a red flag rather than assuming it’s fine.

What to Do

If you have any tejocote root supplement, whether or not you can confirm it’s specifically named on FDA’s list, here’s what to do:

• Stop taking it. Don’t finish the bottle “just to see.”
• Don’t rely on the label alone to reassure you. That’s the entire problem with these products.
• Check the FDA’s current product list for your exact brand and product name.
• If you’ve been taking one of these supplements and are experiencing any symptoms, especially heart palpitations, irregular heartbeat, nausea, vomiting, or neurological symptoms like confusion or vision changes, contact a doctor or seek medical care right away.
• Consider reporting the product to FDA through its MedWatch adverse event reporting program if you experienced a reaction.

You can review the FDA’s full warning, including its current product list, directly at the FDA’s official alert page.

If you’re weighing weight-loss options more broadly and want a safer starting point, our guide on what a GLP-1 actually is covers a regulated, medically supervised alternative. And if you want to understand how supplement contamination issues like this one get caught and reported, our coverage of the Centric Compounding IV wellness recall walks through a similar process from a different corner of the supplement and wellness world.

Frequently Asked Questions

What is tejocote root?

Tejocote root comes from a small tree native to Mexico and Central America and is marketed as a natural weight-loss supplement. It’s sold under various brand names and is often labeled with terms like Raiz de Tejocote, Crataegus mexicana, or Mexican Hawthorn.

What is yellow oleander, and why is it dangerous?

Yellow oleander (Thevetia peruviana) is a poisonous plant that physically resembles tejocote root but is not the same plant. It contains cardiac glycosides, compounds similar to the heart medication digoxin, that can cause neurologic, gastrointestinal, and cardiovascular effects the FDA describes as potentially severe or fatal.

How do I know if my supplement is affected?

Check whether your product’s label references tejocote root, Raiz de Tejocote, Crataegus mexicana, or Mexican Hawthorn, then compare the exact brand and product name against the FDA’s current product list. Pay particular attention if your product is called “D Magic Plus” or “B. Magi,” the two products newly added in the September 17, 2026 update. Because the label won’t disclose the contamination, checking FDA’s list is the only reliable way to confirm.

Is this an official recall?

No. This is an FDA public health warning, not a formal product recall or enforcement action. The FDA is directly warning consumers to stop using these products and continues to test and add products to its list as its investigation proceeds.

What should I do if I’ve been taking one of these products?

Stop taking it. Don’t assume the label is accurate. Check the FDA’s product list for your specific brand, and if you feel unwell, especially with heart palpitations, irregular heartbeat, nausea, or neurological symptoms, contact a doctor or seek medical care right away.

The recall comes from Intercon Chemical Company, and the products shipped to stores and facilities in 15 states. The Food and Drug Administration classified it as a Class II recall on September 11, 2026, meaning the products could cause temporary or reversible health problems.

What Was Recalled

Six specific hand soap products are affected, sold under several different brand names:

Intercon Foaming Pear Hand Soap with Aloe (28.7 fl. oz.) — lots AF97312, 26-01001, and 26-01803

Clearly Better by Intercon Foaming Pear Hand Soap with Aloe (34 fl. oz.) — lots 26-01001 and 26-01803

Summit 150 Foaming Hand Soap (28.7 fl. oz.) — lots BF97303, BF97304, and BF97305

Vestis Foaming Hand Soap, Fresh Pear Scent (33.8 fl. oz.) — lot 26-03091

Laura Lynn Honey Apple Crisp Liquid Hand Soap (8 fl. oz.) — lots C3576 and 26-01804

Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers (7.5 fl. oz.) — lot 26-01001

Laura Lynn is the store brand at Ingles Markets grocery stores, so if you shop at Ingles in the Southeast, that’s the one to check first.

Why It’s Being Recalled

Testing on the soap found several types of bacteria: Pseudomonas aeruginosa, Pseudomonas putida, Pseudomonas monteilii, Serratia marcescens, and Serratia nematodiphila.

These bacteria are most dangerous in healthcare settings. People with weakened immune systems, open wounds, surgical incisions, or medical devices like catheters and ventilators face the highest risk of infection. For most healthy people washing their hands at a bathroom sink, the everyday risk is lower, but the FDA still recalled the product because contaminated soap has no business being sold at all, and vulnerable family members or guests could be exposed without anyone realizing it.

Intercon Chemical Company initiated the recall on June 29, 2026. The FDA’s Class II classification on September 11 confirmed the health risk and made the recall official in the agency’s enforcement database.

Where the Recalled Soap Was Sold

The affected products were distributed to 15 states: California, Georgia, Illinois, Iowa, Maryland, Mississippi, Nebraska, New York, North Carolina, North Dakota, Pennsylvania, South Carolina, Texas, Washington, and Wisconsin.

Because these soaps are sold under different names for different retailers and facilities, it’s possible to have one of them without recognizing the “Intercon” name on the label at all.

What To Do If You Have It

Stop using the soap right away. Check the product name and lot number against the list above, since the lot number is usually printed on the bottom or back of the bottle.

If it matches, don’t keep using it “until it runs out.” Discard the bottle or return it to the store or facility where you got it. If you worry you might have been exposed and you have a weakened immune system, an open wound, or a medical device like a catheter, it’s reasonable to mention it to your doctor.

Frequently Asked Questions

How do I know if I have one of the recalled hand soaps?

Match the product name on your bottle to the six listed above, then check the lot number, usually printed on the bottom of the bottle. If it doesn’t match a listed lot, it isn’t part of this recall.

Is this hand soap dangerous for a healthy person?

The bacteria involved mainly cause infections in people who are already vulnerable — those with weakened immune systems, open wounds, or medical devices like catheters. Healthy people face a lower everyday risk, but the FDA still recommends discarding the product rather than continuing to use it.

What should I do with the recalled soap?

Stop using it immediately and either discard it or return it to the place you purchased it.

Were there any reported illnesses?

No illnesses have been reported in connection with this recall as of the FDA’s Class II classification.

Where can I verify this recall myself?

The FDA publishes all recall classifications, including this one, in its Enforcement Reports database.

Bottom Line

Six hand soap products sold in 15 states are being recalled after bacteria were found inside the bottles. Most healthy people face a modest risk, but if you or someone in your household has a weakened immune system, an open wound, or a medical device, check your soap bottle now and toss it if the lot number matches.

For more on how bacterial contamination shows up in unexpected household and medical products, see our coverage of the Centric Compounding IV vial recall and the broccoli sprouts Salmonella recall.

If you take ramipril for high blood pressure, you’ll want to check your prescription bottle today.

Hikma Pharmaceuticals USA Inc. has recalled a batch of Ramipril Capsules USP, 10 mg. The recall is nationwide within the United States.

The FDA recall number is D-0831-2026. Hikma initiated the recall voluntarily, with a recall initiation date of August 24, 2026, and an FDA report date of September 2, 2026.

Some news outlets covering this recall have reported a figure of more than 28,000 bottles affected. That number comes from press reporting on the recall, not from the FDA’s own enforcement record, so treat it as an estimate rather than a confirmed count.

Why It Matters

The reason for the recall is that the capsules failed impurities and degradation specifications.

In plain terms, testing found the medication had broken down, or contained impurity levels, outside of what the FDA allows. That’s a quality and stability problem with the pills themselves.

The FDA has classified this as a Class II recall. That means the recalled product could cause temporary or medically reversible health problems, or that the chance of serious harm is remote — it is a real safety concern, but not the FDA’s most severe classification.

Ramipril is an ACE-inhibitor medication used by a huge number of adults to manage blood pressure and protect the heart and kidneys. Impurity-related recalls in blood pressure medications have made headlines before, which is part of why this one is getting attention.

What To Do

Go find your ramipril prescription bottle right now.

Check three things: the drug name (Ramipril Capsules, 10 mg), the manufacturer (Hikma Pharmaceuticals USA Inc.), and the strength. If all three match, you likely have a recalled product.

Do not stop taking your blood pressure medication on your own. Suddenly stopping an ACE-inhibitor like ramipril without medical guidance can cause your blood pressure to spike, which carries its own risks.

Instead, call your pharmacist or prescribing doctor. Tell them about the recall and ask about a replacement prescription or an alternative medication while this is sorted out.

You can also verify the recall details yourself using the FDA’s official enforcement report for this recall: FDA Enforcement Report D-0831-2026.

Medication recalls like this one aren’t rare — we also covered a recent nationwide IV medication recall from Centric Compounding over sterility concerns, if you want to see how that one played out for patients.

FAQ

How do I know if I have the recalled bottle?

Look for “Ramipril Capsules USP, 10 mg” manufactured by Hikma Pharmaceuticals USA Inc. on your prescription label. If your bottle shows a different manufacturer or a different strength, it isn’t part of this recall. When in doubt, your pharmacy can check the lot against Hikma’s recall notice.

Is it dangerous?

The FDA classified this as a Class II recall, meaning the risk is generally temporary or reversible rather than life-threatening, though the agency still takes the issue seriously enough to require a nationwide recall. The concern here is that the capsules failed impurity and degradation testing, not that they were mislabeled with the wrong drug.

What do I do?

Check your bottle against the manufacturer and strength above, then contact your pharmacist or doctor to arrange a replacement. Don’t just toss the medication and go without treatment — get a replacement lined up first.

Should I stop taking it immediately?

Don’t stop cold turkey on your own. Talk to your pharmacist or doctor first about switching to a replacement supply, since abruptly discontinuing a blood pressure medication can itself be risky.

Accord Healthcare has recalled five strengths of levothyroxine sodium tablets nationwide because they may not contain the full amount of medication listed on the label.

What Was Recalled

The FDA lists this as a Class II recall, initiated by Accord Healthcare, Inc. on August 6, 2026, and reported to the FDA on September 2, 2026.

Five strengths of levothyroxine sodium tablets, USP, are involved:

• 25 mcg — recall number D-0775-2026
• 50 mcg — recall number D-0776-2026
• 125 mcg — recall number D-0781-2026
• 137 mcg — recall number D-0782-2026
• 200 mcg — recall number D-0785-2026

All five recalls fall under the same FDA enforcement event (event ID 99584). The tablets were distributed nationwide in the United States. This is a voluntary, firm-initiated recall.

You can check the official FDA record, including the recall numbers above, at the FDA’s enforcement report page.

Why It Matters

The reason for the recall is “subpotent drug.” That means the tablets may not contain the full labeled amount of active levothyroxine.

Levothyroxine is a thyroid hormone replacement. Millions of Americans with hypothyroidism take it every day to keep their thyroid hormone levels steady.

If your dose is quietly weaker than what your prescription calls for, your body may not be getting enough thyroid hormone.

That can bring back the exact symptoms your medication is supposed to control: fatigue, weight gain, brain fog, depression, feeling cold, and in more serious cases, heart-related symptoms.

The tricky part is that you would likely still be taking your pill every single day, on schedule, and not know anything is wrong.

You can read more about hypothyroidism and how levothyroxine works from MedlinePlus, a U.S. National Library of Medicine resource.

What To Do If You Take This Medication

Check your bottle. Look at the manufacturer name and lot number on your prescription label. Accord Healthcare is the recalling firm, and this recall covers the 25 mcg, 50 mcg, 125 mcg, 137 mcg, and 200 mcg strengths listed above.

Don’t stop taking it on your own. Suddenly stopping thyroid medication isn’t safe either. Talk to your doctor or pharmacist before you make any change.

Contact your pharmacy. If your bottle matches, ask your pharmacist about getting a replacement from a different lot or manufacturer.

Watch for symptoms. If you’ve noticed new fatigue, weight changes, mood changes, or other symptoms returning, mention it to your doctor, especially if you’re not sure whether your bottle is affected.

If you’ve been dealing with unexplained exhaustion lately, it’s also worth reading our guide on why you’re tired all the time and what you can do about it — fatigue has a lot of possible causes, and a subpotent thyroid prescription is one more thing worth ruling out.

This isn’t the only medication recall we’ve covered recently. If you or a family member has been in the hospital, our writeup on the B. Braun saline recall walks through a separate, unrelated IV product issue.

Frequently Asked Questions

How do I know if I have the recalled lot?

Check the manufacturer name (Accord Healthcare) and the strength on your bottle against the five strengths listed above: 25 mcg, 50 mcg, 125 mcg, 137 mcg, and 200 mcg. Your pharmacist can also look up your specific lot number against the recall.

Is it dangerous to keep taking it?

The concern with a subpotent drug is getting too little thyroid hormone, not too much. That can allow hypothyroidism symptoms to return over time. It is not the kind of recall where you should stop your medication abruptly on your own — talk to your doctor or pharmacist first.

What do I do if my bottle matches?

Contact the pharmacy where you filled the prescription. They can tell you whether your specific lot is affected and help arrange a replacement.

Will I get a refund or replacement?

Your pharmacy is the right place to ask. They handle recalled product returns and replacements directly with the manufacturer or distributor.

Bottom Line

Accord Healthcare recalled five strengths of levothyroxine sodium tablets nationwide because some tablets may be subpotent.

Check your bottle, don’t stop your medication without talking to your doctor or pharmacist, and reach out to your pharmacy if your lot is affected.

Vet Plus, Inc., the company behind the Fi brand, announced this recall on September 3, 2026, with the FDA publishing it on September 8, 2026. The issue traces back to an ingredient supplied to Fi’s manufacturer that may be contaminated with Salmonella.

Two products are affected:

• Fi Calming Supplement for Dogs, 180g, lot 26118
• Fi 8-in-1 Formula Supplement for Dogs, 180g, lot 26159

These were sold direct to consumers through Fi’s website, and through Amazon and Chewy.com.

Why This Recall Matters

Salmonella in pet food and supplements isn’t just a risk to the animal eating it. Pets can carry the bacteria without looking sick, and people who handle contaminated pet products, especially without washing their hands right after, can get sick too.

That risk is highest for children, older adults, pregnant people, and anyone with a weakened immune system. Symptoms in both dogs and people can include diarrhea, vomiting, fever, and lethargy.

As of this recall notice, no illnesses in dogs or humans have been reported.

What To Do If You Have It

1. Check the lot number on your container: 26118 for Calming, 26159 for 8-in-1 Formula.
2. If it matches, stop giving it to your dog right away.
3. Seal the container tightly and throw it in the trash — don’t donate or give it away.
4. Wash your hands thoroughly with soap and water after handling the product or its container.
5. Wash any bowls, scoops, or surfaces that touched the supplement.

If your dog shows signs of illness after eating this product, contact your veterinarian.

Where To Verify This Recall

You can read Vet Plus’s full recall notice directly on the FDA’s website to confirm your lot number before you toss anything.

Frequently Asked Questions

How do I know if my Fi supplement is affected?
Check the lot number on the container. Fi Calming Supplement lot 26118 and Fi 8-in-1 Formula lot 26159 are the only two affected products.

Can Salmonella from dog supplements make people sick, not just pets?
Yes. Salmonella can transfer from contaminated pet products to people who handle them, especially if hands aren’t washed afterward.

Should I take my dog to the vet if they ate the recalled supplement?
If your dog is showing symptoms like vomiting, diarrhea, fever, or lethargy, contact your veterinarian. If your dog seems fine, you can still report the product and dispose of it safely.

Where else was this sold besides Fi’s own website?
The recalled products were also sold through Amazon and Chewy.com.

The Bottom Line

If you have Fi Calming Supplement (lot 26118) or Fi 8-in-1 Formula Supplement (lot 26159) for your dog, check that lot number today. If it matches, stop feeding it, seal it up, and throw it away — and wash your hands after handling it.

For more on pet-related product safety, see our air purifier guide for pet owners and allergy sufferers and our coverage of the Costco jalapeño Salmonella recall.

BMC Medical Co., Ltd. announced a recall on September 7, 2026, and the FDA published it on September 8, 2026. The issue affects the Luna G3 APAP, model LG3600, running firmware version G3-2.00.76.

The FDA has classified this as a Class I recall — the agency’s most serious category, reserved for situations where using the product could cause serious injury or death.

Why This Recall Matters

Here’s the specific failure: when the device is operating under high pressure, a high respiratory rate, and high peak flow at the same time, it can display an error message and then shut itself off automatically.

For anyone using an APAP for sleep apnea, a mid-sleep shutdown means therapy failure exactly when your breathing needs support most. The FDA has not received reports of injury connected to this defect, but the risk is serious enough to warrant its top classification.

How Many Devices Are Affected

BMC says 20,160 devices have already had their firmware updated. But an estimated 196 units may still be running the defective G3-2.00.76 firmware.

The affected devices were manufactured between September 11 and October 18, 2024, and distributed nationwide between October 29, 2024, and July 6, 2026.

What To Do If You Have One

Don’t just stop your therapy without a plan — talk to your doctor first. Here’s the process:

1. Check your device’s firmware version using the serial number lookup tool on BMC Medical’s website (en.bmc-medical.com/rc-adh.html).
2. Contact your physician or your durable medical equipment (DME) provider to discuss next steps.
3. Contact React Health, the U.S. importer, to request a replacement device: 863-226-6285 or 3B-Recall@reacthealth.com.
4. You can also reach BMC Medical directly at bmc-recall@bmc-medical.com.

Support hours for both contacts are Monday through Friday, 8 a.m. to 5 p.m. ET.

Where To Verify This Recall

This is posted as a Class I recall on the FDA’s official recall notice under recall number Z-2979-2026. You can read the full notice directly from the FDA to confirm your device details.

Frequently Asked Questions

How do I know if my CPAP is affected?
Only the Luna G3 APAP, model LG3600, running firmware version G3-2.00.76, is affected. Check your firmware version through BMC’s serial number lookup tool.

Is it safe to keep using my machine while I wait for a replacement?
Talk to your doctor or DME provider before making any changes to your therapy. They can advise you based on your specific device and health needs.

What makes this a Class I recall?
Class I is the FDA’s most serious recall category, used when a product could cause serious health consequences or death. A mid-sleep shutdown during APAP therapy fits that risk profile.

Have there been any reported injuries?
No adverse events have been reported to date, according to the recall notice.

The Bottom Line

If you use a Luna G3 APAP (model LG3600), check your firmware version tonight. If it’s the affected version, contact your doctor and React Health to arrange a replacement before your next night of therapy.

For more on how the FDA handles serious medical device and drug recalls, see our coverage of the B. Braun IV saline recall and the morphine injection mix-up recall.

Galil Importing Corp is recalling Lior Cinnamon Ground Seasoning after a routine sample tested by the Maryland Department of Health came back with elevated levels of lead.

What Was Recalled

The recall covers Lior Cinnamon Ground Seasoning sold in 90 gram clear plastic containers, either individually or in cases of six. Check your container for UPC 794711005484 and lot code GAP11304.

The cinnamon was distributed to retail stores, grocery stores, delis, and supermarkets in New York, New Jersey, Pennsylvania, Texas, Florida, and Illinois. It was sold between November 18, 2025 and September 7, 2026, so it may still be sitting on some store shelves or in home spice cabinets.

Why Lead In Cinnamon Is a Serious Concern

This isn’t the first time ground cinnamon has turned up contaminated with lead. In late 2023, lead-tainted cinnamon in applesauce pouches sickened hundreds of children across the country, some seriously, and led to a wave of related recalls. That outbreak was traced to cinnamon that investigators believe may have been intentionally adulterated to increase its weight and color.

Lead doesn’t cause obvious symptoms right away. It builds up in the body over time, and even low levels of exposure can affect brain development in young children, cause learning and behavior problems, and contribute to high blood pressure and kidney problems in adults. There is no known safe level of lead exposure.

Galil Importing Corp says no illnesses have been reported in connection with this recall so far.

What To Do If You Have This Cinnamon

Stop using it right away.

Throw the container away, or return it to the store where you bought it for a refund. If you have questions, Galil Importing Corp can be reached at 1-516-496-7400, Monday through Friday, 9 a.m. to 5 p.m. Eastern.

If you’re concerned about lead exposure, particularly for a young child who may have eaten food made with this cinnamon, talk to your pediatrician about a blood lead test.

How To Verify This Recall

The full recall notice is posted on the FDA’s website, where you can confirm the product details and check for updates.

If you keep an eye on other pantry recalls, our recent coverage of the Wholesome Pantry apple sauce recall and the Whole Foods cheese recall are both worth a look.

Frequently Asked Questions

How do I know if my cinnamon is affected?

Look for UPC 794711005484 and lot code GAP11304 on your 90 gram Lior Cinnamon Ground Seasoning container. If those match, your product is part of the recall.

How much lead was found?

The recall notice doesn’t specify an exact lead level, only that a sample tested by the Maryland Department of Health showed elevated levels. If you want more detail, you can contact Galil Importing Corp directly.

Is this related to the 2023 cinnamon applesauce recalls?

Not directly. This is a separate recall from a different company. But it’s a reminder that ground cinnamon, especially imported cinnamon, has had recurring lead contamination problems in recent years.

What should I do if I think I’ve been exposed?

Talk to your doctor, especially if a young child in your household regularly ate food made with this cinnamon. A simple blood test can check lead levels.

Berlin Seeds, based in Millersburg, Ohio, is recalling its Alfalfa Sprouting Seed nationwide because it may be contaminated with Shiga toxin-producing E. coli (STEC) and Salmonella.

Berlin Seeds alfalfa sprouting seed is recalled nationwide over possible E. coli and Salmonella.

What Was Recalled

The recall covers Berlin Seeds Alfalfa Sprouting Seed in five package sizes: 1/4 lb., 1/2 lb., 1 lb., 5 lb., and 50 lb.

The 5 lb. and 50 lb. bags carry lot code SAL2-24JB. Smaller package sizes don’t carry a lot code, so if you bought Berlin Seeds alfalfa sprouting seed in any size, it’s covered.

The seed was sold both in stores and online between February 13 and August 23, 2026, and reached nearly every state in the country.

Why It Matters

One illness has already been reported to the company in connection with this seed.

Sprouting seeds carry a higher risk than most other foods because sprouts grow in warm, humid conditions, which are ideal for bacteria to multiply, and they’re almost always eaten raw or lightly cooked. That combination means any contamination on the seed itself can turn into an active infection by the time the sprouts reach your plate.

Both STEC and Salmonella can cause diarrhea, cramping, and fever, and in more serious cases STEC infections can lead to a dangerous kidney complication, especially in young children and older adults.

Check any Berlin Seeds alfalfa sprouting seed in your pantry or garden shelf.

What to Do If You Have It

Stop using the seed immediately. Don’t sprout it, plant it, or eat any sprouts you’ve already grown from it.

Throw the seed away in a sealed bag, or return it to where you bought it. Clean and sanitize any surfaces, containers, or sprouting jars that touched the seed or the sprouts.

If you or anyone in your household has gotten sick after eating homegrown alfalfa sprouts, contact a healthcare provider.

For questions or to arrange a replacement, contact Berlin Seeds at 877-464-0892 or order@berlinseeds.life.

How to Verify This Recall

Read the FDA’s official notice on FDA.gov.

This recall follows a separate, larger multistate sprout outbreak we’ve been tracking. If you want the fuller picture, see our coverage of the Broccoli Sprouts Salmonella outbreak tied to Evergreen Fresh Sprouts.

FAQ

How do I know if my sprouting seed is affected?
If it’s Berlin Seeds brand Alfalfa Sprouting Seed in any package size, it’s covered by this recall. The 5 lb. and 50 lb. bags carry lot code SAL2-24JB.

Is it dangerous to eat sprouts I already grew?
Yes, don’t eat them. Throw away any sprouts grown from this seed along with the unused seed itself.

What if I already ate sprouts from this seed and feel fine?
You’re likely okay, but symptoms of E. coli or Salmonella can take a few days to appear. Watch for diarrhea, cramping, or fever and contact a doctor if they show up.

Is this connected to other sprout recalls I’ve seen this year?
It may be related to the broader sprout contamination issues seen this year, though this is a distinct recall notice for Berlin Seeds’ own seed supply.

What should I do with my sprouting jars and equipment?
Wash and sanitize anything that touched the recalled seed or sprouts grown from it before using it again.

This is the classic Argentinian and Uruguayan style: fresh parsley, garlic, red chili, oregano, olive oil, and red wine vinegar. No blender required, and a little goes a long way.

Key Takeaways

• Ready in 10 minutes with 8 simple ingredients
• Hand chopping gives the best texture, not a blender
• Let it sit at least 15 minutes so the flavors come together
• About 70 to 80 calories per tablespoon, almost all from olive oil
• Keeps in the fridge for up to a week and freezes well

What Is Chimichurri?

Chimichurri is a fresh, uncooked herb sauce from Argentina and Uruguay. It is served with grilled meat at an asado, the South American version of a backyard cookout.

Think of it as a bright, garlicky cousin of salsa or pesto. It is tangy from the vinegar, a little spicy from the chili, and fresh from the parsley.

Why This Chimichurri Recipe Works

• Balanced acid: just enough red wine vinegar to cut through rich meat without making it sour.
• Fresh plus dried herbs: fresh parsley for brightness, dried oregano for that classic earthy flavor.
• Real chili: fresh red chili gives cleaner heat than flakes.
• No cooking: chop, stir, rest, and you are done.

Chimichurri Ingredients

Makes about 1 cup, or 8 servings of 2 tablespoons.

• 1/2 cup olive oil
• 2 tablespoons red wine vinegar
• 1/2 cup fresh flat-leaf parsley, finely chopped
• 3 to 4 garlic cloves, finely chopped or minced
• 2 small red chilies, or 1 larger red chili, seeded and finely chopped (about 1 tablespoon)
• 3/4 teaspoon dried oregano
• 1 teaspoon coarse salt
• 1/2 teaspoon black pepper, or to taste

Ingredient Tips

Parsley: use flat-leaf (Italian) parsley. It has more flavor than curly parsley. Dry it well after washing so the sauce does not get watery.

Red chili: fresh chili gives bright heat. No fresh chili? Use 1/2 to 1 teaspoon of red pepper flakes instead.

Olive oil: a regular extra virgin olive oil is perfect. You do not need anything fancy.

How to Make Chimichurri

Step 1: Chop Everything Fine

Finely chop the parsley, garlic, and red chili with a sharp knife. Add them to a bowl with the salt and pepper.

Hand chopping keeps each piece separate, so the sauce stays bright and textured instead of turning into a paste.

Step 2: Add the Oil, Vinegar, and Oregano

Pour in the olive oil and red wine vinegar, then sprinkle in the oregano. Stir until everything is coated.

Step 3: Let It Rest

Let the chimichurri sit for at least 15 minutes before serving. The garlic mellows, the oregano softens, and the flavors blend together.

Taste it and adjust. Add a pinch more salt if it tastes flat, or a splash more vinegar if it needs brightness.

Step 4: Spoon It Over Your Food

Stir well right before serving, since the oil and herbs separate as it sits. Spoon it over grilled meat, chicken, fish, or vegetables.

What to Serve With Chimichurri

Steak is the classic pairing, especially flank steak, skirt steak, or sirloin sliced thin against the grain. But chimichurri works on almost anything:

• Grilled chicken breasts or thighs
• Salmon, shrimp, or white fish
• Roasted potatoes, zucchini, or bell peppers
• Scrambled or fried eggs
• As a salad dressing. Try it in place of the dressing on our healthy Cobb salad.

If you love South American flavors with beef, our Lomo Saltado recipe is another one to add to your rotation.

Is Chimichurri Healthy?

Yes, with one thing to keep in mind. Chimichurri is made from herbs, garlic, vinegar, and olive oil, with no added sugar and almost no carbs.

The calories come from the olive oil. This batch works out to roughly 70 to 80 calories per tablespoon, so portion matters if you are working on your first 10 pounds.

The good news: one tablespoon packs a lot of flavor. Spoon it on instead of pouring it, and a plate of grilled chicken and roasted vegetables goes from boring to steakhouse good for under 100 extra calories.

Easy Variations

• Milder: remove all the chili seeds, or use half the chili.
• Extra fresh: swap a quarter of the parsley for cilantro.
• Brighter: add a squeeze of lemon juice with the vinegar.
• Smoky: add a pinch of smoked paprika.
• Red chimichurri: stir in a spoonful of finely chopped roasted red pepper.

How to Store Chimichurri

Fridge: store it in a sealed jar in the refrigerator for up to 1 week. Because it contains fresh garlic in oil, always keep leftovers refrigerated.

Freezer: spoon it into an ice cube tray, freeze, then move the cubes to a freezer bag. Each cube is about one serving, ready to thaw whenever you need it.

Before serving: the olive oil firms up in the fridge. Let it sit out for 15 to 20 minutes, then stir.

Frequently Asked Questions

Can I use dried parsley?

Fresh parsley is what makes chimichurri taste like chimichurri. Dried parsley will work in a pinch, but the sauce will be much less vibrant.

Can I make chimichurri in a food processor?

Yes, but pulse only a few times. Too much blending bruises the parsley and turns the sauce into a dull green paste.

Can I use chimichurri as a marinade?

Yes. Set aside some fresh sauce for serving first, then use the rest to marinate meat for 30 minutes to a few hours. Never reuse marinade that touched raw meat.

Is chimichurri spicy?

This version has a gentle kick from the red chili. Remove the seeds or use less chili if you want it milder.

What is the difference between chimichurri and pesto?

Chimichurri uses parsley and vinegar and has no cheese or nuts. Pesto uses basil, Parmesan, and pine nuts, so it is richer and higher in calories.

Bottom Line

This chimichurri recipe is one of the easiest ways to make healthy dinners taste exciting. Ten minutes of chopping gives you a week of bright, garlicky flavor for steak, chicken, fish, and vegetables.

Make a batch this weekend, keep it in the fridge, and use a spoonful whenever dinner needs a lift. Then try it on our healthy Cobb salad for lunch.

Shine Bright.

Everything Sprouts LLC, a Minneapolis-based grower, has recalled several of its sprout products after they were linked to a multistate outbreak of E. coli and Salmonella. As of the latest count, 55 people across 15 states have gotten sick. Four people were hospitalized.

What makes this recall drag on is the seed. The FDA traced the outbreak back to a shared seed lot, and for weeks the seed supplier wouldn’t agree to a recall of its own. That changed on September 15, 2026, when the supplier finally recalled the implicated seed lot, closing the loop on where the contamination started.

What Was Recalled

The recall covers several 5-ounce sprout products sold under the Everything Sprouts and Calco brand names:

• Everything Sprouts Alfalfa Sprouts
• Calco Alfalfa Sprouts
• Everything Sprouts Crunchy Protein Sprout Mix
• Everything Sprouts Zesty Garlic Mix
• Everything Sprouts Robust Radish Sprout Mix

The affected lot numbers are 222, 223, 225, 226, 230, and 233, depending on the product. You’ll find the lot number printed on the container near the use-by date.

The products were distributed in Florida, Indiana, Iowa, Kansas, Michigan, Minnesota, New Hampshire, New York, North Carolina, North Dakota, Pennsylvania, South Carolina, South Dakota, Washington, and Wisconsin, though sprouts often travel further than their original distribution list once they reach grocery stores and food service accounts.

Why This Recall Matters

Sprouts are one of the riskiest raw vegetables you can eat, and this outbreak shows why.

Seeds are grown in warm, humid conditions that are ideal for bacteria like E. coli and Salmonella to multiply. Because sprouts are eaten raw, there’s no cooking step to kill off contamination the way there is with most other produce.

This outbreak has sickened 55 people since illnesses tied to it began showing up in late May. Forty-six people were infected with E. coli, seven with Salmonella, and two people caught both. That combination of two different pathogens from the same seed source points to contamination at the source, not a one-off kitchen mistake.

What To Do If You Have This Product

If you have any Everything Sprouts or Calco sprout product in your fridge, check the label.

Do not eat it. Sprouts can’t be made safe by rinsing, and while cooking to 165 degrees Fahrenheit can reduce risk, the FDA and CDC recommend simply not eating raw sprouts from a recalled lot at all.

Throw the product away in a sealed bag, or take it back to the store where you bought it for a refund. Afterward, wash and sanitize your refrigerator shelves, drawers, and any containers that may have touched the sprouts, since both E. coli and Salmonella can spread to other foods through cross-contamination.

If you or someone in your household ate the recalled sprouts and is now dealing with severe stomach cramps, bloody diarrhea, vomiting, or a fever over 102 degrees, contact a healthcare provider. E. coli symptoms can take up to 10 days to appear after exposure, so don’t assume you’re clear just because a few days have passed without symptoms.

Frequently Asked Questions

How do I know if I have the recalled sprouts?

Check the brand name (Everything Sprouts or Calco) and the lot number on the container, which should be one of 222, 223, 225, 226, 230, or 233. If you’re not sure where you bought your sprouts or can’t find a lot number, the safer move is to throw them out.

Is this recall connected to the broccoli sprouts recall from Evergreen Fresh Sprouts?

No. These are two separate outbreaks involving two different companies. Evergreen Fresh Sprouts, based in Idaho, recalled broccoli sprouts tied to a Salmonella Bovismorbificans outbreak. This recall involves Everything Sprouts LLC in Minnesota and a shared alfalfa seed lot linked to both E. coli and Salmonella. If you eat sprouts regularly, it’s worth checking both recalls.

What are the symptoms of E. coli and Salmonella?

E. coli symptoms typically include severe stomach cramps, watery or bloody diarrhea, and vomiting, usually starting three to four days after exposure but sometimes taking up to 10 days. Salmonella symptoms include diarrhea, fever, and stomach cramps, usually appearing within six hours to six days of eating contaminated food. Most people recover without treatment, but young children, older adults, pregnant people, and anyone with a weakened immune system are at higher risk of severe illness.

Is it safe to eat any sprouts right now?

Sprouts from lots outside this recall are not affected. If you’re unsure, contact the store or brand directly, or consider skipping raw sprouts for now if you’re in a higher-risk group. It’s also worth double-checking recent Salmonella-linked produce recalls like the Costco jalapeño recall if you buy a lot of fresh produce.

Where can I find the official recall notice?

The FDA’s outbreak investigation page has the full case count, timeline, and updates as the investigation continues. The CDC also lists E. coli symptoms and prevention guidance.

Bottom Line

Fifty-five illnesses and four hospitalizations later, this recall is a reminder that raw sprouts carry real risk, and that a slow-moving seed supplier can keep an outbreak going longer than it needs to. Check your fridge for the affected lot numbers, toss what you find, and watch for symptoms if you’ve already eaten any.