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CL Answer

Which supplements help to improve energy and decrease fatigue?

Energy supplements and vitamins - Some can help increase energy and reduce fatigue, including CoQ10, curcumin/turmeric, cocoa, and B vitamins.

Product Review

Dark Chocolates, Cocoa & Cacao Powders, Nibs, and Supplements Review -- Sources of Flavanols

Is Your Chocolate or Cocoa Healthful or Toxic? Find the Best Dark Chocolate, Cocoa Powder and Cocoa Supplements Based On Our Tests.

News Release

March 13, 2025

Best L-Glutamine Supplements According to ConsumerLab Tests

White Plains, NY, March 13, 2025 —  L-glutamine (glutamine) supplements are promoted to boost energy and the immune system and for other benefits, but do they really work, and if so, which glutamine products on the market are best?

Recalls & Warnings

December 07, 2016

Chocolate Hazelnut Butter CLIF Nut Butter Filled Energy Bars Recalled

On November 18, 2016, Clif Bar & Company issued a recall of one production run of Chocolate Hazelnut Butter CLIF Nut Butter Filled energy bars due to the presence of small plastic pieces found in a limited number of bars.

News Release

February 26, 2025

ConsumerLab Survey Shows 21 Most Popular Vitamins and Supplements

White Plains, New York, February 26, 2025 — A recent survey of more than 8,400 people who regularly use dietary supplements shows that among the 212 most popular supplements, those that experienced the greatest absolute growth in popularity during 2024 were biotin (+9.

CL Answer

Can eating almonds reduce wrinkles or have other health benefits?

Find out if eating almonds can reduce wrinkles or improve aging skin.

CL Answer

I have type 2 diabetes. Should I be concerned about ingredients like maltodextrin and maltitol that are found in some protein bars and drinks?

Learn more about maltitol and maltodextrin and their effects on blood glucose levels for people with type 2 diabetes.

News Release

December 16, 2022

Is Your Chocolate or Cocoa Healthful or Toxic? ConsumerLab Finds Major Differences Among Products.

White Plains, New York, December 16, 2022 — Although dark chocolate and cocoa can be good sources of potentially heart-healthy, antioxidant flavanols, they can also be contaminated with toxic heavy metals such as cadmium and lead – and consumers can’t judge products from their labels.

Product Review

Baobab Dried Fruit Pulp Review Article

What Are the Benefits of Baobab Dried Fruit Pulp? Find Out What's In Baobab Super Fruit Products, Safety, Side Effects & More.

CL Answer

Energy Gels: What Are They Used For and Do They Contain Their Labeled Ingredients?

Energy gels are a convenient on-the-go carbohydrate source, but some products may not contain the amount of carbohydrates stated on the label.

CL Answer

What are sugar alcohols and why are they in my nutrition bar?

Learn more about sugar alcohols, including maltitol and lactitol, why some products contain them, and possible side effects.

News Release

June 14, 2022

Best B Complexes, B12, and Other B Vitamin Supplements Revealed by ConsumerLab Tests: Beware of High Doses

  White Plains, New York, June 14, 2022 — Recent ConsumerLab tests of over 30 popular vitamin B complexes and supplements revealed that four products contained either much less, or much more, of at least one B vitamin listed on the label.

News Release

November 05, 2021

NAD Boosters for Energy and Memory? ConsumerLab Reviews NAD+, NAHD and NMN Supplements

White Plains, New York, November 5, 2021 — Most cells in the body use NAD (nicotinamide adenine dinucleotide) in the process of energy production, and compounds that boost blood levels of NAD are often sold in supplements marketed for a wide range of benefits, from increasing energy and ...

CL Answer

How much caffeine is really in dark chocolate bars?

Just how much caffeine is really in chocolate bars? Get our test results on the caffeine content in dark chocolate and cocoa powder.

CL Answer

How much dark chocolate equals a tablespoon of cocoa powder?

Learn how much dark chocolate will give you the same intake of flavanols as a tablespoon of cocoa powder.

News Release

June 16, 2021

Wide Variations in Ginseng Potency, Quality Revealed by ConsumerLab Tests

White Plains, New York, June 16, 2021 — Ginseng is promoted for a wide range of uses, from increasing energy, "vitality," and libido, to improving blood sugar levels and preventing colds.

CL Answer

Is Hershey's Special Dark better than other dark chocolate bars or cocoa powders?

Find out if Hershey's Special Dark Chocolate bar is better than other dark chocolate bars or cocoa powders, including flavanol content, contamination with lead or cadmium and other tests of quality. ConsumerLab.com's answer explains.

CL Answer

5 Tips for Finding a Soap or Body Wash That Won't Irritate Skin

Get 5 tips for finding soap or body wash that won't cause skin irritation. See which soaps we rate best, ingredients to avoid, and phrases on labels that can mislead.

CL Answer

Does methylene blue increase energy, slow aging, or improve memory?

Methylene blue is promoted for increasing energy, slowing aging, and improving memory. Find out if there is evidence for this, plus safety and side effects.

CL Answer

What are the health benefits of dark chocolate?

Information on the health benefits of dark chocolate, including how dark chocolate may improve heart health, decrease blood sugar levels and more. ConsumerLab.com's answer explains.

CL Answer

How much fat is there in chocolate? Is it saturated fat?

Learn more about the fat content in dark chocolate & milk chocolate, how much is saturated, and serving size.

CL Answer

How can I find supplements that are gluten-free on ConsumerLab.com?

Gluten-Free supplements & vitamin information including other dietary features like vegetarian, vegan, and kosher on ConsumerLab.com. Our answer explains.

News Release

January 23, 2020

We Found the Best Dark Chocolates and Cocoas With the Least Contamination

White Plains, New York, January 23, 2020 — Dark chocolate and cocoa contain antioxidant flavanols that may be good for the heart and mind, but they can also contain high levels of the heavy metal cadmium, which is toxic to kidneys and can soften bones.

News Release

September 11, 2019

Some Nutrition Bars Contain More Carbs and Less Fiber Than Listed, ConsumerLab Tests Reveal

White Plains, New York, September 11, 2019 — Nutrition bars and cookies are promoted as a convenient way to get protein, fiber and other nutrients on-the-go, but recent ConsumerLab tests of popular nutrition bars and cookies reveal that some contain more carbohydrates (as well as fat and ...

News Release

March 07, 2019

Best Coconut and MCT Oils Identified by ConsumerLab

White Plains, New York, March 7, 2019 — Coconut oil is often promoted as a "healthy fat" and an alternative source of energy to help with weight loss and in conditions such as Alzheimer's disease because it contains medium chain triglycerides (MCTs).

News Release

July 19, 2017

New Tests Reveal Whether Dark Chocolates and Cocoas Are Toxic or Healthful

White Plains, New York, July 19, 2017 — Dark chocolates and cocoa may contain dangerously high levels of the heavy metal cadmium, a kidney toxin, according to recent tests conducted by ConsumerLab.com, an independent evaluator of health and nutrition products.

CL Answer

Is there a risk of liver toxicity with certain supplements?

Find out if there is risk of liver damage from supplements such as green tea, niacin, red yeast rice and vitamin A.

CL Answer

Why is there so much cadmium, a toxin, in cocoa powders but not in dark chocolate?

Learn more about the presence of the toxic heavy metal cadmium in cocoa powder and dark chocolate.

CL Answer

Can taking too much vitamin B-6 be dangerous?

Find out if multivitamins contain excessive amounts of B-6, how much B-6 is too much, and symptoms of toxicity and overdose.

CL Answer

Should I be concerned about phytic acid in oat cereals? I've heard that it can be harmful, but also that it can have health benefits.

Get information on phytic acid levels found in oats and oat cereals.

CL Answer

Which supplements can cause diarrhea?

Can supplements like magnesium cause diarrhea? Find out which supplements may cause diarrhea, such as vitamin B12, curcumin, magnesium, vitamin C and fish oil.

CL Answer

I thought the B vitamins were all water soluble and did not build up in the body, so you would not build up toxic levels. Am I wrong?

Learn more about water-soluble B vitamins including niacin, B6, B12 and folic acid, and why taking too much of these vitamins can be toxic. See the symptoms of overdose and toxicity from B vitamins. ConsumerLab.com's answer explains.

Recalls & Warnings

January 31, 2021

Protein and Fiber Bars Recalled Due to Allergen Risk

On January 28, 2021, think! and Interpac Technologies, Inc. issued a voluntary recall of think! Protein + Fiber Oatmeal: Farmer's Market Berry Crumble due to the potential presence of tree nuts, including almonds and pecans.

CL Answer

Can taking too much vitamin B-12 be dangerous? The label on my B-complex states it contains 50,000% of the Daily Value!

Find out the daily value for vitamin B-12 and the potential side effects of taking too much B-12. ConsumerLab explains why taking too much vitamin B-12 can be harmful.

CL Answer

I'm over 50 and looking to take a vitamin B-12 supplement. Many contain a form of vitamin B-12 called cyanocobalamin, yet I read on the Internet that this form is toxic. Should I be concerned?

Looking to see if the cyanocobalamin form of vitamin B-12 is safe? Read research and safety information on ConsumerLab's report.

CL Answer

Is the theobromine in chocolate and cocoa good or bad for me?

Find out the benefits and risks of theobromine -- and how much is in dark chocolate.

CL Answer

Does Gynostemma pentaphyllum really work as an AMPK activator and help for diabetes, high cholesterol, or weight loss?

Find out if Gynostemma pentaphyllum ( jiaogulan) works as an AMPK activator and helps to lower blood sugar and treat diabetes. ConsumerLab.com's answer explains.

News Release

March 05, 2015

ConsumerLab.com Shows Chinese Consumers What's Really in Foods and Supplements -- U.S. Testing Company Expands to China, Launches cn.ConsumerLab.com

White Plains, New York, March 5, 2015 — Since 1999, American consumers and doctors have turned to ConsumerLab.com (CL) to find out which nutritional products are highest in quality based independent testing. Today, CL launched a Chinese-language website cn.ConsumerLab.

News Release

December 09, 2014

Round-up of Recent Product Tests by ConsumerLab.com -- Results for B Vitamin Supplements & Energy Drinks, Garlic, NAC (N-acetyl cysteine), Iron and Omega-7 Fatty Acids

White Plains, New York, December 9, 2014 — In recent months, ConsumerLab.com has published test results for a variety of popular supplements, including B vitamins supplements and energy drinks, NAC (N-acetyl cysteine), iron and garlic. In addition, ConsumerLab.

News Release

November 25, 2014

You Can't Judge a Dark Chocolate Bar by Its Label, According to Tests by ConsumerLab.com -- Amounts of Cocoa Flavanols Vary Widely Among Popular Brands of Chocolate

White Plains, New York, November 25, 2014 — Which dark chocolates provide the most cocoa flavanols — natural antioxidants associated with better blood flow and memory? Recent tests by ConsumerLab.

News Release

October 08, 2013

ConsumerLab.com Reports Problems and “Top Picks” Among Bars for Energy, Fiber, Protein, Meal-Replacement, and Whole Food

WHITE PLAINS, NEW YORK — October 8, 2013 — Which nutrition bars provide the best combination of nutrition and taste, and are accurately labeled? ConsumerLab.com recently set out to answer this question by purchasing popular bars in the U.S.

News Release

June 11, 2013

31% of Protein Powders and Drinks Fail Tests by ConsumerLab.com

White Plains, New York — June 11, 2013 — What's really in a scoop of "protein powder"? sIn some products, a lot less protein or a lot more carbohydrates than you would expect, and perhaps even a serving of something you don't want -- lead. That's according to recent tests by ConsumerLab.

News Release

September 27, 2012

ConsumerLab.com Reveals How Much Caffeine is in Energy Drinks -- Also Finds Some Drinks and Dietary Supplements Don't Contain Claimed Amounts of B Vitamins

White Plains, New York — September 27, 2012 — Energy shots and drinks are promoted to keep you alert and energized, attributing their effects to special formulas often "packed with B vitamins and nutrients to make it last," as a commercial for 5-hour Energy proclaims.

News Release

February 05, 2012

Fish oil and multivitamins most popular supplements in ConsumerLab.com survey -- Internet most popular place to shop

WHITE PLAINS, NEW YORK — FEBRUARY 5, 2012 — A survey of over 10,000 savvy consumers of supplements shows the most popular supplements to be fish oil, multivitamins, vitamin D, calcium and CoQ10, in that order.

CL Answer

Bee pollen: Purported health benefits and possible side effects

Bee pollen is promoted for numerous health conditions, including supporting immune health and boosting energy. Find out if it works and if it's safe.

CL Answer

Adrenal Fatigue and Adrenal Support Supplements: Do they work and are they safe?

Find out what's really in supplements for adrenal support and adrenal fatigue, including herbal adrenal support supplements and bovine derived adrenal support supplements. Find out if they really work and if they are safe. ConsumerLab.com's answer explains.

CL Answer

Is it true that iodine can cause acne or other skin problems?

Information on iodine causing acne and other skin problems such as rashes and hives. ConsumerLab.com's answer explains.

CL Answer

What are the health benefits of chlorophyll and chlorophyllin, and are they safe?

Chlorophyll supplements are promoted for reducing body odor, preventing cancer, removing toxins from the body, improving digestive conditions and other uses, but do they work and are they safe? Find out and learn if such supplements actually contain chlorophyll.

CL Answer

What is Marine-D3 with Seanol-P, and does it live up to anti-aging claims?

Learn about the evidence for Marine-D3, a supplement from Marine Essentials that contains Seanol, including evidence from clinical studies on aging.

News Release

October 26, 2010

ConsumerLab.com reports deficiencies in some B-complex supplements and more caffeine than expected in "shot-sized" B vitamin "energy" drinks

White Plains, New York — October 26, 2010 — Tests of B vitamin supplements, including B-complexes and shot-sized energy drinks, revealed problems with the quality of 4 out of 18 products selected for review by independent testing organization ConsumerLab.com.

News Release

May 05, 2010

Tests of protein powders and drinks show some lead contamination but no melamine -- New report covers whey, soy, and rice protein supplements for body building, endurance/recovery, meal-replacment and dieting

WHITE PLAINS, NEW YORK — MAY 5, 2010 — New tests by ConsumerLab.com found most protein powders, shakes and drinks to meet their nutrient claims, but two products were contaminated with lead (6 to 18 mcg per day) and a third product contained four extra grams of sugar.

CL Answer

Is it okay to take vitamin D3 and fish oil together?

Find out if taking vitamin D and fish oil is okay, how it effects absorption, and the best way to take vitamin D to improve absorption. ConsumerLab.com's answer explains.

CL Answer

Which supplements or OTC medications help reduce flatulence (gas), and are there any that make it worse?

Find out which supplements may help reduce flatulence (gas), and learn which supplements or foods may worsen symptoms of flatulence.

CL Answer

Which air purifiers are best for reducing microbial and smoke particles from room air?

Find out if portable air cleaners can remove the virus that causes COVID-19 infection from the air and learn which type air cleaners work best.

CL Answer

Butyrate Supplements for Gut Health: Does butyric acid really work and is it safe?

Can butyrate supplements improve gut health or help reduce symptoms of irritable bowel syndrome (IBS) or Crohn's disease? Find out what the clinical evidence shows, learn about the different forms of butyrate, including sodium butyrate, calcium-magnesium butyrate, and tributyrate, and get details about products such as BodyBio Sodium Butyrate and Healus Complete Biotic Tributyrin, dosage, safety and cost.

CL Answer

What does "%DV" (Daily Value) mean on a supplement label, how does it differ from RDAs, and should anyone take more than the DV for a nutrient?

Find out the difference between RDAs (Recommended Daily Allowances) and DVs (Daily Values) for vitamins and minerals, and learn whether certain groups of people should take more than the 100% DVs for vitamins and minerals.

Recalls & Warnings

June 07, 2013

Nutrition Bars Recalled Due To Undeclared Milk Allergen

On June 6, 2013, Sequel Naturals Ltd. issued a recall of Vega sports, nutrition and energy bars because they contain undeclared milk. Consumption of these bars can cause serious or life-threatening reactions in people with an allergy to milk.

Recalls & Warnings

June 14, 2013

Protein And Nutrition Bars Recalled Due To Undeclared Milk Allergen

On June 13, 2013, the U.S. FDA alerted consumers that Sequel Naturals Ltd., dba Vega, issued a voluntary recall of a variety of Vega One and Vega Sport protein bars because the bars contain undeclared milk.

Recalls & Warnings

April 10, 2021

HI-TECH Workout Supplements Recalled Due to Undeclared Allergens

On April 3, 2021, HI-TECH Pharmaceuticals issued a recall of all lots of APS Nutrition Isomorph 28 in a 2lb jug because they contain undeclared milk, wheat, and soy.

Recalls & Warnings

June 02, 2016

Clif Bars Recalled Due to Listeria Risk

On June 2, 2016, Clif Bar & Company issued a recall of certain energy and trail mix bars because they contain sunflower kernels which have the potential to be contaminated with Listeria monocytogenes. 

Recalls & Warnings

October 15, 2012

Recall of Nutrition Bars Containing Peanut Butter Due To Salmonella Risk

On October 11 and 12, 2012, four brands of nutrition bars were voluntarily recalled due to possible salmonella contamination of the peanut butter used in each of these bars. The peanut butter was produced by Sunland Inc., and is part of a larger recall of Sunland's peanut butter and peanut products.

News Release

August 12, 2008

ConsumerLab.com finds improvements in labeling of nutrition bars but potential pitfalls exist -- New report compares 20 bars, including those for protein, fiber, energy and whole food

WHITE PLAINS, NY — August 12, 2008 — Labeling on nutrition bars has become more accurate, according to a new report by ConsumerLab.com.

Recalls & Warnings

January 13, 2025

NuGo Nutrition Bar Recall Expanded

On January 10, 2025, Lifestyle Evolution Inc. expanded its recall of NuGo Dark Chocolate Chip nutrition bars to include NuGo Dark Chocolate Pretzel nutrition bars and nutrition bar multipacks, due to an undeclared milk allergen.

Recalls & Warnings

December 10, 2024

Nu Go Nutrition Bars Recalled

On December 3, 2024, Wegmans announced a recall of Nu Go Dark Chocolate Chocolate Chip Nutrition Bar due to an undeclared milk allergen.

News Release

August 20, 2007

ConsumerLab tests products in booming nutrition drink market — most deliver what's promised but extra cholesterol found in some — New report covers drinks and powders for endurance/recovery, body building, meal-replacement and dieting

WHITE PLAINS, NEW YORK — AUGUST 20, 2007 — A new report from ConsumerLab.com finds most nutrition powders, shakes and drinks meet their nutrient claims, but three products — two sports drinks and a meal supplement — contained more cholesterol than claimed.

Recalls & Warnings

April 04, 2025

Tony’s Chocolonely Dark Chocolate Bars Recalled

On April 1, 2025, Tony’s Chocolonely Inc. recalled seven lots of its Dark Chocolate Almond Sea Salt Bar and Everything Bar due to the potential presence of small stones.

News Release

July 17, 2007

Concerned by weaknesses in FDA's new rules for dietary supplements, ConsumerLab.com acts to "raise the bar on quality"

WHITE PLAINS, NEW YORK — July 17, 2007 — Disappointed by the lack of quality standards within the FDA's newly released Good Manufacturing Practices (GMPs) for dietary supplements, ConsumerLab.com has announced two initiatives today intended to "raise the bar on quality.

Recalls & Warnings

January 24, 2009

Many Brands of Nutrition Bars Recalled Due to Potential Salmonella Contamination

Due to salmonella contamination in peanut butter produced by Peanut Corporation of America, manufacturers of nutrition and snack bars made with this material have recently issued voluntary recalls.

Recalls & Warnings

January 31, 2002

Recall Update for Certain Metabolife Bars - Excessive Vitamin A

The U.S. Food and Drug Administration (FDA) released the following Class I recall information in its January 30, 2002 Enforcement Report.

News Release

June 20, 2005

Quality problems widespread among ginseng products sold in Japan. — Nearly two-thirds of products fail ConsumerLab.com testing due to pesticide contamination and missing or substandard ingredients

WHITE PLAINS, NY — JUNE 20, 2005 — Among 14 brands of ginseng dietary supplements recently purchased in Japan and tested by ConsumerLab.com, only 5 products passed independent testing by ConsumerLab.com.

News Release

February 08, 2005

ConsumerLab.com reports on nutrition bars — Highlights major differences, inaccuracies, and urges consumers to "know your bar"

WHITE PLAINS, NY — February 8, 2005 — ConsumerLab.com reported test results today for 34 nutrition bars, including those designed for high protein, low-carb/diet, energy, or meal-replacement.

Recalls & Warnings

January 03, 2024

FDA Warns Amazon for Selling Men’s Supplements Containing Prescription Drugs

On December 20, 2023, the FDA issued a Warning Letter to Amazon.com, Inc.

News Release

January 09, 2004

USANA products pass ConsumerLab.com screening for substances banned from Olympics

WHITE PLAINS, NY — January 9, 2004 — ConsumerLab.com announced today that six additional products have passed its Athletic Banned Substances Screening Program. ConsumerLab.com tested the products at the request of USANA, a supplement manufacturer. ConsumerLab.

News Release

August 28, 2003

Some problems persist with ginseng supplements but overall quality improves according to ConsumerLab.com — Test results published online today

WHITE PLAINS, NY — August 28, 2003 — In contrast to its testing three years ago in which nearly 60% of Asian and American Ginseng supplements were found to have significant problems, testing of recently purchased products by ConsumerLab.

Recalls & Warnings

December 13, 2023

Bobo’s Peach Oat Bars Recalled Due to Undeclared Coconut

On December 9, 2023, Bobo’s issued a nationwide recall of multiple lots of Bobo’s Peach Oat Bars because they may contain undeclared coconut.

Recalls & Warnings

May 22, 2023

Hu Vanilla Crunch Dark Chocolate Bars Recalled Due to Allergen Risk

On May 18, 2023, Hu Products issued a voluntary recall of one lot of its Vanilla Crunch Dark Chocolate Bar because they may contain undeclared tree nuts (hazelnut, cashew, and/or almond).

News Release

March 05, 2002

ConsumerLab.com finds nutrition powders & drinks more accurately labeled than nutrition bars, but unapproved food ingredient seen in some

White Plains, NY -- March 5, 2002 — ConsumerLab.com announced today that 24 of 26 nutrition powders and drinks that it recently evaluated met their label claims for carbohydrates, fats, and proteins. This is in stark contrast to ConsumerLab.

News Release

October 30, 2001

Sixty percent of nutrition bars fail to meet claims in ConsumerLab.com tests — "Low Carb" bars often loaded with carbohydrates; excess sodium and saturated fat also found

WHITE PLAINS, NY — October 30, 2001 — ConsumerLab.com, an independent evaluator of dietary supplements and nutrition products, released results today of its Nutrition Bar Product Review.

News Release

August 15, 2001

Problems and ambiguity among alternative estrogen products reported by ConsumerLab.com — Results of soy and red clover isoflavone product testing released online today

WHITE PLAINS, NY — August 15, 2001 — ConsumerLab.com, an independent evaluator of dietary supplements and nutrition products, today released results of its Phytoestrogen Product Review. The review focused on dietary supplements made from soy and red clover isoflavones.

Recalls & Warnings

August 25, 2023

FDA Warns Consumers Not to Use Big Guys Male Energy Supplement

On August 22, 2023, the FDA warned consumers not to buy or use BIG GUYS Male Energy Supplement after FDA laboratory analysis found it to contain undeclared sildenafil.

Recalls & Warnings

June 17, 2024

Do Not Consume Diamond Shruumz Products, Warns CDC and FDA

On June 12, 2024, the Center for Disease Control and Prevention (CDC), Food and Drug Administration (FDA), and America’s Poison Centers warned consumers not to buy or consume Diamond Shruumz chocolate bars, cones, and gummies.

Recalls & Warnings

April 29, 2024

Longreen Reishi and Xlim Express Coffee Recalled Due to Undeclared Allergens

On April 18, 2024, BF Suma Pharmaceuticals, Inc.

Recalls & Warnings

June 17, 2022

Built Brand Protein Bar Recalled Due to E. Coli Concern

On June 10, 2022, Built Brands, LLC. Issued a recall of 4,146 Banana Cream Pie Puffs protein bars after routine testing discovered potential contamination with E. coli (Escherichia coli).

News Release

July 09, 2001

Many herbal sleep products lack key claimed ingredient — Results of ConsumerLab.com's testing of valerian products released on web today

WHITE PLAINS, NY — July 9, 2001 — ConsumerLab.com, an independent evaluator of dietary supplements and nutrition products, today released results of its Product Review of valerian supplements — used primarily as sleep aids and minor tranquilizers.

Recalls & Warnings

April 03, 2023

SimplyProtein Bars Recalled Due to Undeclared Cashews

On March 31, 2023, Wellness Natural USA Inc. issued a voluntary recall of a single lot of SimplyProtein Peanut Butter Chocolate Crispy Bars because they contain undeclared trace of tree nuts (cashews).

Recalls & Warnings

May 22, 2023

Nature’s Energy Children’s Colostrum Recalled Due to Undeclared Milk

On May 18, 2023, Nature’s Energy issued a recall of six lots of Children’s Chewable Colostrum products due to undeclared milk.

Recalls & Warnings

February 03, 2025

Four Male Enhancement and Energy Supplements Found to Contain Drugs

On January 16, 2025, the FDA issued a Warning Letter to Mihon Corp. d/b/a VitalityVita and Boulla, LLC after FDA analysis found four of the company’s supplements, VitalityXtra, PeakMax, ZapMax, and ZoomMax, to contain undeclared sildenafil.

Recalls & Warnings

April 17, 2024

FDA Warns Lipari Foods for Mislabeled Walnuts, Other Violations

On April 9, 2024, the FDA issued a Warning Letter to Lipari Foods Operating Company, LLC following multiple complaints and subsequent product recalls in August and September of 2023, which found the company did not follow the requirements of Current Good Manufacturing Practice (CGMP), Hazard ...

Recalls & Warnings

May 09, 2024

Walnuts, Other Nuts, Pumpkin and Sunflower Seeds Recalled Due to Undeclared Allergens

On May 8, 2024, Texas Pecan recalled various lots of the company’s 1 lb. and 8 oz.

Recalls & Warnings

September 23, 2024

Lactaid Milk Recalled Due to Allergen

On September 20, 2024, HP Hood LLC voluntarily recalled five SKUs of refrigerated Lactaid Milk due to the product potentially containing trace amounts of almond, which is not declared on the label. No illness has been reported to date.

Recalls & Warnings

October 10, 2024

Seaweed Recalled Due to Allergen Risk

On October 10, 2024, Wismettac Asian Foods, Inc. recalled its 3.52 oz packages of Shirakiku Korean Seasoned Seaweed.

Recalls & Warnings

September 03, 2019

Federal Court Shuts Down Two Supplement Companies Selling Weight, Joint Health and Other Supplements

On September 3, 2019, a U.S. District Court entered a consent decree of permanent injunction against Basic Reset and Biogenyx, two Tennessee-based companies that sell dietary supplements and other product promoted for health benefits.

Recalls & Warnings

November 17, 2022

FDA Warns Consumers Not to Use Male Enhancement Supplement

On November 10, 2022, the FDA warned consumers not to buy or use Sangter Natural Male Energy Supplement after FDA laboratory analysis confirmed the presence of undeclared sildenafil.

Recalls & Warnings

January 16, 2023

Sanders Dark Chocolate Sea Salt Caramels Recalled Due to Plastic

On December 30, 2022, the Canadian Food Inspection Agency announced the recall of certain lots of Sanders Candy Dark Chocolate Sea Salt Caramels due to pieces of plastic being found in products.

Recalls & Warnings

August 03, 2022

Sexual Enhancement Supplement Recalled Due to Sildenafil

On August 1, 2022, DISTRIBUTOR RFR, LLC recalled one lot of SANGTER Energy Supplement 3000 mg to the consumer level after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

Recalls & Warnings

May 01, 2023

TruVision Recalls Products Due to Presence of Potentially Dangerous Ingredients

On April 27, 2023, TruVision Health issued a recall of various dietary supplement products because they contain hordenine and/or octodrine/DMHA, compounds that the FDA considers to be “possibly unsafe” and which are not permitted to be sold as dietary supplements.

Recalls & Warnings

September 06, 2023

WEFUN Capsules Recalled Due to Undeclared Sildenafil

On August 25, 2023, WEFUN Inc. issued a recall of 300 boxes of WEFUN Capsules after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

Recalls & Warnings

May 04, 2023

FDA Warns MedoLife for Promoting Homeopathic Products to Treat COVID-19, Cancer

On April 19, 2023, the FDA issued a warning letter to Medolife Rx D/B/A MedoLife Corp., AELIA Inc. and Queanta Inc.

Recalls & Warnings

December 04, 2023

Manischewitz Dark Chocolate Coins Recalled Due to Undeclared Milk

On December 1, 2023, Manischewitz issued a recall of one lot of Manischewitz Dark Chocolate Coins because they contain undeclared milk. The recalled lot of coins are labeled as “dark chocolate,” but contain milk chocolate coins.

News Release

June 04, 2001

ConsumerLab.com reports test results of arthritis supplement — MSM; Quality found higher than for most supplements, but room for improvement remains

WHITE PLAINS, NY — June 4, 2001 — ConsumerLab.

News Release

May 07, 2001

Over forty percent of Echinacea products fail ConsumerLab.com review; Inadequate labeling and missing ingredients found common for popular herbal cold remedy

WHITE PLAINS, NY — May 7, 2001 — ConsumerLab.com, an independent evaluator of dietary supplements and nutrition products, today released results of its Product Review of echinacea supplements.

News Release

April 10, 2001

Quality of popular herbal anti-depressant found to vary; certain types of St. John's Wort supplements more likely to pass testing

White Plains, NY — April 11, 2001 — ConsumerLab.com, an independent evaluator of dietary supplements and nutrition products, today released results of its Product Review of St. John's wort supplements.

News Release

March 27, 2001

ConsumerLab.com expands testing of health products; success of dietary supplement evaluations leads company into broader nutrition field, beginning with popular nutrition bars

WHITE PLAINS, NY — March 27, 2001 — Having established its presence as the leading independent evaluator of the quality of dietary supplements sold in the U.S, ConsumerLab.com announced today the expansion of its work to include foods and food ingredients.

Recalls & Warnings

October 03, 2020

Some "Dairy-Free" Dark Chocolate Found to Contain Undeclared Milk

On October 1, 2020, the FDA announced findings from a study it conducted from 2018 to 2019 that showed that some dark chocolate products claiming to be "dairy-free" or "milk-free" contain undeclared milk.

Recalls & Warnings

June 23, 2020

BioPure Healing Products Warned for Manufacturing Violations

On June 17, 2020, the FDA issued a warning letter to BHP Holdings Inc.

Recalls & Warnings

January 11, 2023

Male Sexual Enhancement Supplement Found to Contain Prescription Drug

On January 9, 2022, the FDA issued a warning letter to Distributor RFR, LLC after laboratory analysis of the company’s SANGTER Natural Male Energy Supplement found the product to contain undeclared sildenafil, a prescription medication.

Recalls & Warnings

March 09, 2022

Court Bars Salud Natural From Selling Aloe, Joint Supplements & More

On March 8, 2022, a federal court ordered Salud Natural Entrepreneur, Inc. to stop distributing nutritional supplements that violate the Federal Food, Drug and Cosmetic Act (FDCA).

Recalls & Warnings

May 09, 2022

Natural Organics Keto Capsules Recalled Due to Gluten

On March 6, 2022, Natural Organics, Inc. issued a recall of four lots of NaturePlus Keto Living Sugar Control Capsules that were found to contain gluten.

Recalls & Warnings

August 20, 2024

Two Sexual Enhancement Supplements Sold on Amazon Recalled

On August 20, 2024, Veata LLC Endurance Pro Energy Boost capsules and Boulla LLC Boom Max capsules were recalled because they contain sildenafil, a prescription medication which is not permitted in dietary supplements.

Recalls & Warnings

August 28, 2024

Now Foods Recalls Raw Brazil Nuts Due to Mold and Yeast

On August 14, 2024, NOW Foods issued a recall of its Now Foods Whole & Unsalted Raw Brazil Nuts because they were found to be contaminated with mold and yeast.

Recalls & Warnings

July 19, 2024

Walnuts Recall Due to Listeria

On July 19, 2024, Stutz Packing Company recalled its 1-pound packages of Shelled Walnuts due to potential contamination of Listeria monocytogenes. Routine sampling realized that the finished products contained bacteria. Currently, there have been no reports of illness related to this call.

Recalls & Warnings

December 26, 2024

Sleep Supplement Recalled Due to Undeclared Soy

On October 30, 2024, Deseret Biologicals Inc. recalled 2,547 bottles of DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, which are labeled as containing phosphatidylserine from sunflower lecithin powder but contain undeclared soy lecithin.

Recalls & Warnings

April 17, 2025

Spermidine Supplement Sold on Amazon Recalled

On April 14, 2025, Supplement Manufacturing Partners, Inc. recalled Dorado Nutrition brand Spermidine Maximum Strength 10 MG per serving because it contains undeclared wheat. The mislabeled product was discovered after a Supplement Manufacturing Partner investigation tested the product.

News Release

March 13, 2001

ConsumerLab.com review of vitamin E supplements finds some insufficiencies and need for clearer labeling; test results released online today

WHITE PLAINS, NY — March 13, 2001 — ConsumerLab.com today released results of its Product Review of vitamin E products. Vitamin E is one of the most popular dietary supplements in the U.S.

Recalls & Warnings

June 15, 2016

More Nutrition Bars Recalled Due to Listeria Risk

The following nutrition bars are being recalled because they contain sunflower kernels or may have come in contact with equipment processing sunflower kernels which have the potential to be contaminated with Listeria monocytogenes (use the links below for affected lot numbers, UPC, and/or ...

Recalls & Warnings

December 08, 2020

Dark Chocolate Recalled Due to Allergen Risk

On December 1, 2020, Maribel's Sweets issued a recall of Cacao Market Cylinder Dark Chocolate Pearls because they contain undeclared milk.

Recalls & Warnings

June 16, 2020

Seller of Silver, Arginine, and More Warned for Manufacturing Violations

On June 1, 2020, the FDA issued a warning letter to Morningstar Minerals LLC, which found the company's products, including Silver Boost, to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

Recalls & Warnings

April 18, 2022

Moringa Concern: Blood Clots

A 63-year-old woman in New York with type 2 diabetes developed a blood clot in the lungs (i.e. pulmonary embolism) that her physicians suspect may have been caused by the use of a supplement containing Moringa oleifera extract (Ebhohon, Int J Emerg Med 2022).

Recalls & Warnings

March 19, 2009

QVC Settles Charges of False Claims for Supplements

On March 19, 2009, the Federal Trade Commission (FTC) announced that QVC, Inc., a TV home shopping channel and one of the world’s largest multimedia retailers, has agreed to pay $7.

Recalls & Warnings

February 14, 2020

Dark Chocolate Bar Recalled Due to Allergen Risk

On February 13, 2020, Gourmet International and Butlers Chocolates UC issued a recall of IRISH WHISKEY DARK CHOCOLATE 3.5OZ TABLET BAR chocolate bars because they may contain undeclared milk.

Recalls & Warnings

March 24, 2020

Mislabeled Lindt Chocolate Bar Recalled

On March 19, 2020, Lindt & Sprüngli (USA) Inc. issued a recall of one lot of Lindt Excellence 85% Cocoa chocolate bars because they are wrapped in the wrong packaging.

Recalls & Warnings

October 02, 2020

Tonic Therapeutic Herb Shop & Elixir Bar Warned for COVID-19 Claims

On September 29, 2020, the FDA issued a warning letter to Tonic Therapeutic Herb Shop & Elixir Bar for selling various herbal products, including Tonic Therapeutic Herb Shop & Elixir Bar, with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

May 10, 2021

Whole Food's 365 Everyday Value Whey Protein Recalled

On May 7, 2021, Arizona Nutritional Supplements issued a recall of 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor because it contains undeclared soy. Containers of 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor were mistakenly packaged with Soy Protein Powder.

Recalls & Warnings

June 14, 2023

Havasu Beet Root Powder Recalled Due to Allergen Risk

On June 12, 2023, Supplement Manufacturing Partner Inc. issued a recall of one lot of Havasu Nutrition’s Beet Root Powder + due to undeclared milk. The recall was initiated following a report of an allergic reaction from a consumer with a milk allergy.

Recalls & Warnings

June 19, 2023

A&Z Pharmaceutical Warned for Promoting Calcium & Vitamin D for Hair Loss, Osteoporosis & Cancer

On June 1, 2023, the FDA issued a warning letter to A&Z Pharmaceutical, Inc. following inspection of the company’s website and social media, which found statements about the company’s Chewable Calcium 600MG with Vitamin D for Kids in Orange Flavor products to be drug claims.

Recalls & Warnings

June 22, 2023

Nationwide Pharmaceutical’s Ferrous Sulfate Supplements Recalled

On June 22, 2023, the U.S.

Recalls & Warnings

August 16, 2023

FDA Warns Sellers of Homeopathic Products for Infants and Children

On August 9, 2023, the FDA issued a warning letter to ALVA-AMCO Pharmacal Companies, LLC and CalmCo LLC, previously named Ketomi LLC, following a review of the company websites, which found statements about company homeopathic products to be drug claims because they are intended to diagnose, cure, ...

Recalls & Warnings

July 24, 2023

ONO Overnight Oats Recalled Due to Allergen Risk

On July 18, 2023, ONO LLC issued a voluntary recall of the company’s ONO Vegan Blueberry Muffin Protein Overnight Oats due to undeclared milk.

Recalls & Warnings

November 30, 2023

Original The Rock Capsules Recalled Due to Undeclared Sildenafil

On October 18, 2023, Noah’s Wholesale, LLC issued a nationwide recall of one lot of the company’s Original The Rock capsules after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

Recalls & Warnings

January 15, 2024

5 Star Nutrition Will Pay $4.5 Million for Selling Misbranded Workout Supplements

On January 12, 2024, Defyned Brands, also known as 5 Star Nutrition LLC, pleaded guilty in federal court to three-counts of distributing misbranded dietary supplements following an investigation by the Food and Drug Administration’s Office of Criminal Investigations (FDA-OCI).

Recalls & Warnings

August 07, 2023

Aerosol Bed Bug & Flea Killer Recalled Due to Injury Risk

On August 3, 2023, Maggie’s Farm issued a recall of the company’s Aerosol Bed Bug & Flea Killer products because the aerosol can can rupture and expel shrapnel, posing an injury and laceration hazard to consumers.

Recalls & Warnings

October 09, 2023

Orgain Protein Powder Recalled Due to Allergen Risk

On October 4, 2023, Orgain LLC issued a recall of four lots of the company’s Organic Protein Powder + Superfoods, Creamy Chocolate Fudge flavor protein powder after a co-manufacturer informed the company that the product contained undeclared sesame, which is now one of nine food ...

Recalls & Warnings

February 15, 2013

Energy Drink Recalled Due To Bacterial Contamination

On December 21, 2012, NBTY issued a voluntary recall of the energy supplement MET-Rx Extreme Thermo Rage Watermelon 8 fl. oz. (Manufactured by MET-Rx Nutrition, Inc.) due to bacterial contamination.

Recalls & Warnings

July 12, 2019

PROBAR Meal Bars Recalled

On July 11, 2019, PROBAR LLC issued a recall of certain flavors and lots of its Meal® bars because they may contain undeclared milk and soy allergens. There has been one report of an allergic reaction to-date.

Recalls & Warnings

June 20, 2019

Weight Loss, Muscle & Energy Supplements Linked to Adverse Events in Children and Young Adults

Consumption of dietary supplements sold for weight loss, muscle building, and energy are associated with an increased risk for severe medical events in children and young adults compared to the consumption of vitamins, according to a recent study published in the Journal of the Adolescent ...

Recalls & Warnings

January 24, 2020

Fat-Burning, Energy Supplement Linked to Heart Trouble

A 33-year-old woman in Australia developed cardiac ischemia (a lack of blood flow to the heart) after taking the "fat burning" supplement Alpha Lean-7, according to a recent report in the Journal of Sports Sciences.

Recalls & Warnings

March 04, 2021

Federal Court Bars Confidence USA from Selling Supplements

On March 4, 2021, the FDA announced a permanent injunction has been entered, barring dietary supplement manufacturer Confidence USA Inc. and two of its executives from producing or selling products until they become compliant with current good manufacturing practices (cGMPs).

Recalls & Warnings

August 17, 2021

Love & Peas Protein Rich Meal Replacement Recalled

On July 30, 2021, Nature's Sunshine issued a recall of certain lots of Love & Peas Protein Rich Meal Replacement because it may contain milk.

Recalls & Warnings

May 09, 2022

$149 Million in Refunds from AdvoCare Settlement

On May 5, 2022, the FTC announced it will be returning more than $149 million to individuals who sold AdvoCare supplements as distributors through the company’s multi-level-marketing (MLM) plan.

Recalls & Warnings

August 08, 2022

Woman Pleads Guilty for Selling and Promoting Products to Treat COVID-19

On July 27, 2022, Diana Daffin, owner of Savvy Holistic Health pleaded guilty to selling products with claims they could treat COVID-19 and promised “Immunity for Humans.” The products were sold under the HAMPL brand name.

Recalls & Warnings

January 25, 2021

Washington Resident Arrested for Selling Illegal COVID-19 Vaccine

On January 21, 2021, 55-year-old Washington resident Johnny T. Stine was arrested for selling and administering illegal, home-made COVID-19 vaccines to Americans.

Recalls & Warnings

January 21, 2021

Federal Court Bars Fusion Health From Promoting Vitamin D for COVID-19

On January 8, 2021, the United States Department of Justice announced a permanent injunction has been entered, barring dietary supplement marketer Matthew Ryncarz and his companies Fusion Health and Vitality LLC dba Pharm Origins and Fusion Ionz LLC dba Pharm Origins from making claims that their ...

Recalls & Warnings

July 10, 2020

Seller of Thrive "Anti-Viral" Supplement Barred from Making Unproven Coronavirus and Cancer Claims

On July 10, 2020, the Federal Trade Commission (FTC) barred marketer Marc Ching from making unsubstantiated claims that the supplement Thrive can treat, prevent, or reduce the risk of coronavirus (COVID-19). Thrive consists mainly of vitamin C and herbal extracts.

Recalls & Warnings

October 19, 2020

Seller of Thrive "Anti-Viral" Supplements Settles with FTC for Unproven Coronavirus and Cancer Claims

On October 19, 2020, the Federal Trade Commission (FTC) approved an administrative consent order to settle charges that marketer Marc Ching was making unsubstantiated claims that the supplement Thrive can treat, prevent, or reduce the risk of coronavirus (COVID-19).

Recalls & Warnings

May 10, 2016

Multis and Energy Mixes Recalled

On May 9, 2016, Let's Talk Health, Inc. issued a recall of the following supplements because they contain the undeclared allergens soy and milk: 

Recalls & Warnings

January 20, 2019

RXBAR Protein Bars Recalled

On January 15, 2019, RXBAR issued a recall of certain varieties of protein bars because they may contain undeclared peanuts.

Recalls & Warnings

March 30, 2019

Sea Salt 70% Dark Chocolate Bar Recalled Due to Allergen Risk

On March 28, 2019, Theo Chocolate issued a recall of 3oz Sea Salt 70% Dark Chocolate bars because they may contain undeclared milk. 

Recalls & Warnings

January 19, 2022

FDA Warns Seller of Carnitine and Alpha Lipoic Acid Supplements

On November 18, 2021, the FDA issued a warning letter to GeroNova Research Inc.

Recalls & Warnings

May 24, 2021

U.S. Marshals Seize $1.3 Million Worth of Kratom

U.S. Marshals have seized approximately $1.3 million worth of bulk kratom and kratom supplements manufactured by Atofil, LLC, a subsidiary of Premier Manufacturing Products, according to the FDA.

Recalls & Warnings

November 09, 2021

Five Brands of Protein Supplements Recalled Due to Allergen Risk

On November 9, 2021, Nutracap Holdings, LLC issued a recall of certain Boba Origin, Etedream, RAW, Steel, and Vital Force protein supplements because they contain potential allergens, including soy, milk, wheat, and/or coconut, that are not declared on the label.

Recalls & Warnings

June 22, 2021

Living Free Vitamins, Joint, Nerve and Other Supplements Recalled

On June 21, 2021, Bea Lydecker's Naturals, Inc. issued a recall of six Living Free brand supplements because the labels do not declare soy lecithin.

Recalls & Warnings

February 26, 2020

Company Failed to Report Adverse Events Associated With Its Nutrition Shakes

On February 12, 2020, the FDA sent a warning letter to Market America Inc for failure to submit serious adverse event reports about two of its products, as required by federal regulation. The company received two reports following serious adverse events but did not submit the proper forms:

Recalls & Warnings

February 18, 2020

Seller of CoQ10, Resveratrol and More Warned for Manufacturing Violations

On February 5, 2020, the FDA issued a warning letter to R-Garden LLC, which found the company's Vitamin O, Gamma-Zyme, L.

Recalls & Warnings

October 05, 2019

Advocare to Pay $150 Million to Settle Charges of Operating a Pyramid Scheme

AdvoCare International, the marketing company that sells Spark energy drink, as well as other nutrition products and supplements, has agreed to settle FTC charges that it operated an illegal pyramid scheme.

Recalls & Warnings

December 21, 2019

Supplement Company Continues to Make False Claims About Its Products, Says FTC

The FTC has filed a motion of contempt against two supplement companies that, according to the motion, have continued to promote their products with false claims despite being barred from doing so by a previous court order.

Recalls & Warnings

January 24, 2013

"Thermo Stimulating" Supplement Recalled -- Contained DMAA

On January 23, 2013, Health Canada advised consumers not to use certain batches of Muscletech Hydroxystim capsules which were found to contain DMAA (1,3-dimethylamylamine) and have been recalled by their distributor.

Recalls & Warnings

March 30, 2021

Real Water Alkaline Water Recalled for Possible Link to Liver Illness

On March 24, 2021, Real Water, Inc. recalled all sizes of Real Water bottled alkaline water because it may be linked to multiple cases of non-viral hepatitis that occurred in Las Vegas, NV in November of 2020.

Recalls & Warnings

June 05, 2020

Seller of CBD, Sleep Aids, and Cold & Flu Products Warned for Manufacturing Violations

On April 28, 2020, the FDA issued a warning letter to The Dragontree Apothecary LLC, which found the company's Sleep Support, Anxiety Relief, Cold & Flu Relief, and Inflammation Relief to be adulterated because they were prepared, packed, or held under conditions that ...

Recalls & Warnings

June 02, 2020

Sundial Herbal Ordered to Halt Distribution of Products

On June 1, 2020, a New York federal judge filed an order against two individuals doing business as Sundial Herbal Products to stop the company from distributing its products, which were found to be misbranded and promoted as drugs.

Recalls & Warnings

December 11, 2020

Colloidal Silver Seller Warned for COVID-19 Claims

On December 2, 2020, the FDA issued a warning letter to Heavenly Natural Products for selling various Carbon 60 and colloidal silver products, including AVOCADO C60 ANTI-VIRAL COMBO — VIRUS PREVENTION (made with C60 WITH AVOCADO and Heavenly Silver) with unsupported ...

Recalls & Warnings

December 11, 2020

Seller of "Dr. Hotze's Immune Pak" Products Warned for COVID-19 Claims

Seller of "Dr. Hotze's Immune Pak" Products Warned for Coronavirus Claims 

Recalls & Warnings

December 11, 2020

FDA Warns iThrive.health for Promoting Supplements as COVID-19 Treatments

On December 10, 2020, the FDA issued a warning letter to iThrive.health for promoting the sale of various vitamins and supplements on Amazon.com with claims that they can mitigate, prevent, treat, diagnose, or cure COVID-19.

Recalls & Warnings

August 13, 2020

FDA Warns Seller of Chaga for Coronavirus Claims

On August 6, 2020, the FDA issued a warning letter to Canadian Chaga for selling 124 Chaga Capsules, Chaga Tea, and Canadian Chaga Tincture with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

August 10, 2020

Seller Indicted for Promoting Silver Product as Coronavirus Cure

On July 28, 2020, Utah resident Gordon Pedersen was indicted by a federal grand jury for posing as a medical doctor to sell an unapproved treatment for coronavirus (COVID-19).

Recalls & Warnings

July 31, 2020

FTC Sues Golden Sunrise for Marketing Deceptive $23,000 Coronavirus Cure

On July 31, 2020, the Federal Trade Commission (FTC) charged Golden Sunrise Nutraceutical, Inc., a California-based company, with deceptively advertising a $23,000 treatment plan as a scientifically proven way to treat COVID-19.

Recalls & Warnings

July 28, 2020

Iron Supplements Recalled Due to Undeclared Allergen

Between July 23 and 24, 2020, two companies issued recalls of iron supplements because they may contain undeclared milk.

Recalls & Warnings

July 17, 2020

Sellers of Immune Boosters, Vitamin C Warned for Coronavirus Claims

The FDA recently issued warning letters to two companies for selling products such as immune boosters, vitamin C, and zinc with unsupported claims that they can treat COVID-19 (use the links below to read the full warning letter):

Recalls & Warnings

November 02, 2020

Silver Cannot Be Promoted to Prevent or Treat COVID-19

On October 30, 2020, the FDA issued a warning letter to Spartan Enterprises Inc. dba Watershed Wellness Center for selling the silver product Dissolve BioActive Silicate with unsupported claims that it can treat coronavirus (COVID-19).

Recalls & Warnings

October 30, 2020

Seller of Vitamin C, Vitamin D, Ashwagandha, and More Warned for COVID-19 Claims

On October 23, 2020, the FDA issued a warning letter to Predator Nutrition for selling the products Elixir, Salidroside, Unbreakable, Vitamin C + Bioflavonoids & Rosehip, Vitamin D3, and Ashwagandha with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

October 30, 2020

Seller of Elderberry and Honey Products Warned for COVID-19 Claims

On October 23, 2020, the FDA issued a warning letter to Beepothecary LLC for selling the products BEEHive Delight, BEEbread, and Elderberry, Honey & Propolis Syrup with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

October 30, 2020

Simple Silver Cannot Be Promoted to Prevent or Treat COVID-19

On October 23, 2020, the FDA issued a warning letter to Peterson Research Laboratories LLC for selling the product Simple Silver with unsupported claims that it can treat coronavirus (COVID-19).

Recalls & Warnings

May 12, 2020

FTC Halts Deceptive Supplements & Cosmetics "Free Trial" Scheme

On May 8, 2020, the owners of AH Media Group, LLC agreed to halt their allegedly deceptive practice of luring consumers with supposed "free trial" offers for cosmetics and dietary supplements, then enrolling them in subscriptions and billing them without their consent.

Recalls & Warnings

May 09, 2020

Federal Court Orders Seller to Stop Promoting Silver Product as Coronavirus Cure

On April 29, 2020, a federal court in Utah announced that it has obtained a temporary restraining order preventing Gordon Pedersen and his companies, My Doctor Suggests LLC and GP Silver LLC, from promoting fake treatments for coronavirus (COVID-19).

Recalls & Warnings

October 12, 2020

Griffo Botanicals Warned for COVID-19 Claims

On October 7, 2020, the FDA issued a warning letter to Griffo Botanicals for selling various herbal products, including BaseCamp, Gan Mao, Febris, Fortifend, Xiao Chai Hu, HuBei #1, Qing Fei Pai Du, Solis, and WuHan #2, with unsupported claims that they can treat coronavirus ...

Recalls & Warnings

October 12, 2020

Prairie Dawn Herbs Warned for COVID-19 Claims

On October 7, 2020, the FDA issued a warning letter to Prairie Dawn Herbs for selling various herbal products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

August 16, 2013

Maker of Energy, Weight Loss, Sleep and Vitamin D Supplements Warned for Manufacturing Violations

On July 22, 2013, the FDA issued a warning letter to N.V.E. Pharmaceuticals, Inc.

Recalls & Warnings

November 04, 2016

Energy Drink Linked to Case of Acute Hepatitis

A case of acute hepatitis has been linked to daily consumption of energy drinks, according to a report published on November 1, 2016, in BMJ Case Reports.

Recalls & Warnings

April 06, 2018

EXO Cricket Protein Bars Recalled

On April 5, 2018, Aspire Food Group, issued a recall of certain 60 gram EXO cricket protein bars because they may contain undeclared sulfites. Apricots used in the products contain sulfur dioxide as a preservative.

Recalls & Warnings

January 16, 2018

Adverse Effects From Energy Drinks Common Among Youth and Young Adults

More than half (55.4%) of young people who have ever consumed an energy drink have experienced at least one adverse reaction, according to study published yesterday in CMAJ Open, a journal of the Canadian Medical Association.

Recalls & Warnings

February 13, 2018

American College of Sports Medicine Warns of Energy Drink Dangers

A new statement released by the American College of Sports Medicine (ACSM) highlights the dangers of energy drinks when consumed by children and adolescents, and calls for more studies on the safety and efficacy energy drinks.

Recalls & Warnings

November 27, 2017

Protein Bars Recalled After Consumer Finds Piece of Plastic in Bar

On November 23, 2017, Leclerc Foods recalled one lot of Fit & Active Chocolatey Chip Protein Meal Bars distributed to ALDI stores, as a precautionary measure after a small piece of yellow plastic was discovered by a consumer.

Recalls & Warnings

March 31, 2018

Nutrition Bars Sold at Whole Foods and Online Recalled

On March 26, 2018, eBars LLC, issued a recall of their Protein Bars, Snack Bars, and Kids Bars because they may contain undeclared peanuts and/or almonds.

Recalls & Warnings

March 06, 2018

Protein Bars Recalled Due to Undeclared Allergens

On March 5, 2018, IDLife, LLC, issued a recall of their Protein Bars, Snack Bars, and Kids Bars because they may contain undeclared almonds, peanuts, and/or coconut oil.

Recalls & Warnings

July 16, 2016

Ikea Expands Recall of Chocolate Bars

On July 6, 2016, IKEA expanded its recall of certain CHOKLAND chocolate bars to include additional chocolate bars, including certain GODIS chocolate bars, because they contain undeclared milk, hazelnuts and/or almonds.

Recalls & Warnings

October 12, 2018

Organic Plant Protein Shake Recalled

On October 11, 2018, Forager Project issued a recall of certain Nuts and Vanilla — Organic Plant Protein Shakes because the products contain almond flour which is not declared on the label.

Recalls & Warnings

March 05, 2020

Protein Powder Recalled Due to Undeclared Milk

On March 3, 2020, New Capstone, Inc. issued a recall of ReStructure Vanilla Protein Powder because it may contain undeclared milk.

Recalls & Warnings

March 28, 2014

Nutrition Bars Recalled Due to Allergen Risk

On March 27, 2014, Clif Bar & Company issued a voluntary recall of a small number of 15-count boxes of Chocolate Chunk LUNA Bars because they contain undeclared macadamia nut butter.

Recalls & Warnings

January 14, 2017

Dark Chocolate Bar Recalled Due to Allergen Risk

People with an allergy to milk these bars as they could cause an allergic reaction, which can be life-threatening. Recalled Chip'n Dipped Dark Chocolate Crunch chocolate bars were distributed nationwide in retail stores and can be identified by the following:

Recalls & Warnings

July 05, 2017

CLIF Bars Recalled Due to Allergen Risk

On July 5, 2017, CLIF Bar & Company issued a voluntary recall of CLIF BUILDER'S Bar Chocolate Mint, CLIF Kid Zbar Protein Chocolate Mint, and CLIF Kid Zbar Protein Chocolate Chip flavors due to the potential presence of peanuts and tree nuts, including almonds, Brazil nuts, cashews, ...

Recalls & Warnings

March 11, 2013

Nutrition Bar Recalled Due To Undeclared Allergen

On March 7, 2013, Lifestyle Evolution Inc. issued a recall of various NuGO nutrition bars because the bars may contain undeclared milk, a potential allergen.

Recalls & Warnings

August 17, 2012

Voluntary Recall of Nutrition Bars

On August 13, 2012, Clif Bar & Company issued a voluntary recall of a limited amount of 12-pack Blueberry Crisp Clif Bars and individual Blueberry Crisp Clif Bars which were mislabeled in Chocolate Chip Clif Bar wrappers.

Recalls & Warnings

May 06, 2017

Herbalife Protein Bar Recalled

On May 1, 2017, Herbalife issued a recall of certain lots of its Protein Bar -- Peanut Butter nutrition bars because it may contain a trace amount of fish gelatin which contains a small amount of parvalbumin, a fish allergen.

Recalls & Warnings

December 13, 2016

Case of Hemorrhagic Stroke Linked to Redline Energy Drink

A case of hemorrhagic stroke has been linked to the consumption of a single energy drink, according to a report published on October 11, 2016, in The American Journal of Emergency Medicine.

Recalls & Warnings

October 13, 2016

Soylent Recalls Bars As It Investigates Complaints of Gastrointestinal Issues

On October 12, 2016, Soylent announced it is halting all Soylent Bar purchases and shipments while it investigates consumer complaints of gastrointestinal issues, such as vomiting and diarrhea, after consuming the bars.

Recalls & Warnings

April 01, 2017

Nutrition Bar Recalled Due to Allergen Risk

On March 30, 2017, Lifestyle Evolution issued a recall of one shift of NuGo Slim Crunchy Peanut Butter nutrition bars because a product with a milk allergen was incorrectly packaged into some NuGo Slim Crunchy Peanut Butter wrappers and cartons.

Recalls & Warnings

July 02, 2016

Ikea Recalls Dark Chocolate Bars Due to Allergen Risk

On June 24, 2016, IKEA issued a recall of certain CHOKLAD MÖRK and CHOKLAD MÖRK 70% dark chocolate bars because they contain undeclared milk, hazelnuts and almonds.

Recalls & Warnings

July 11, 2017

Gluten Free Chocolate Chip Bars Recalled Due to Allergen Risk

On July 10, 2017, Coborn's, Inc. recalled packages of Gluten Free Chocolate Chip Bars because some were incorrectly labeled as Gluten Free Fudge Brownies.

Recalls & Warnings

March 28, 2017

Yogurt Peanut Crunch Bars Recalled Due to E. Coli Risk

On March 23, 2017, Pro Sports Club of Bellevue, WA issued a recall of 36,957 20/20 Life Styles Yogurt Peanut Crunch bars because they have the potential to be contaminated with Escherichia coli O157:H7.

Recalls & Warnings

February 12, 2015

Many Dark Chocolate Bars Found to Contain Undeclared Milk

On February 11, 2015, the FDA announced its study of dark chocolate bars found many - including some which did not list milk as an ingredient or were labeled as "dairy-free" or "allergen-free," to contain milk.

Recalls & Warnings

November 11, 2015

Consuming a Single Energy Drink May Increase Cardiovascular Risk

A recently published study found that consumption of a single caffeinated energy drink significantly increased blood pressure and noradrenaline levels in healthy young adults. The researchers noted these changes could potentially increase the risk of cardiovascular events.

Recalls & Warnings

December 13, 2017

Dark Chocolate Bar Recalled

On December 8, 2017, ALDI, in cooperation with Hofer KG ZNL Schokoladefab, recalled Choceur Dark Chocolate Bars due to the potential presence of almond pieces not listed on packaging. These bars can cause an allergic reaction in people who have a nut allergy.

Recalls & Warnings

August 03, 2017

Protein Bars Recalled Due to Listeria Risk

On August 2, 2017, Amrita Health Foods recalled several varieties of protein bars due to potential contamination with Listeria monoocytogenes.

Recalls & Warnings

April 25, 2017

Soylent Powder Recalled Due to Allergen Risk

On April 24, 2017, Soylent issued a recall of 890 boxes (containing 7 x 15 oz pouches) of Soylent 1.8 Powder, because the product may contain undeclared milk.

Recalls & Warnings

June 17, 2017

Protein Bars and Bites Recalled Due to Listeria Risk

On June 15, 2017, Bulletproof 360, Inc. recalled five Collagen Protein Bar and Bite products because of potential contamination with Listeria monocytogenes.

Recalls & Warnings

October 13, 2016

Nutrisystem Bars Recalled Due to Listeria Risk

On October 11, 2016, Nutrisystem Everyday, LLC issued a recall of one lot of its Nutricrush Chocolate Chip Cookie Dough bar because it has the potential to be contaminated with Listeria monocytogenes.

Recalls & Warnings

August 31, 2012

Energy, Fat Loss Supplement Recalled For Ephedrine Alkaloids

On August 28, 2012, dietary supplement re-sale distributor Brand New Energy (BNE) issued a recall of EphBurn 25 after FDA testing found the product to contain ephedrine alkaloids.

Recalls & Warnings

January 16, 2013

Nutrition Bars Recalled Due To Undeclared Allergen

On January 15, 2012, Belmont Confections Inc. issued a voluntary recall of Dymatize Nutrition Elite Gourmet Cookies & Cream bars and Dymatize Nutrition Elite Gourmet Fudge Brownie bars because they may contain undeclared peanuts.

Recalls & Warnings

November 21, 2012

Distributor Warns of Counterfeit Liquid Energy Shots

On November 19, 2012, Living Essentials LLC announced the company discovered and halted the production of counterfeit versions of 5-hour ENERGY® liquid energy shots. The company filed suits against the counterfeiters in U.S.

Recalls & Warnings

July 11, 2011

Use of "Sports Drinks" and "Energy Drinks" Discouraged by Pediatric Group

A report from the American Academy of Pediatrics outlines how sports and energy drinks are being misused and provides guidance to decrease or eliminate consumption by children and adolescents.

Recalls & Warnings

March 06, 2013

Protein Bar Recalled Due To Salmonella Risk

On March 4, 2013, Pro-Amino International Inc. issued a recall of Proti Diet High Protein Chocolate Dream Bar due potential Salmonella contamination.

Recalls & Warnings

July 29, 2017

Increase in Calls to Poison Control Centers About Supplements

The number of calls to poison control centers in the U.S. about dietary supplement exposures increased by almost 50% between 2005 and 2012, according to a study published this week in the Journal of Medical Toxicology.

Recalls & Warnings

July 24, 2017

Protein Bars Recalled Due to Listeria Risk

On July 21, 2017, Bhu Foods recalled a number of their products after their organic sunflower seeds, distributed by Hudson Valley Foods, Inc., were potentially contaminated with Listeria monoocytogenes.

Recalls & Warnings

November 19, 2018

Jay Robb Egg White Protein Recalled

On November 16, 2018, Jay Robb Enterprises issued a recall of its Unflavored Egg White Protein Product because it may contain undeclared milk.

Recalls & Warnings

September 22, 2018

MyoWhey Protein Powder Recalled

On September 20, 2018, Purus Labs, Inc. issued a recall of one lot of MyoWhey Chocolate Cookie Crunch protein powder because it may contain undeclared milk and soy.

Recalls & Warnings

April 27, 2018

Labrada LeanPro8 Protein Powders Recalled Due to Allergen Risk

On April 24, 2018, Labrada Nutrition issued a recall of certain lots of LeanPro8 protein powders because they may contain undeclared egg protein.

Recalls & Warnings

June 03, 2019

Vinpocetine May Cause Miscarriage or Fetal Harm

Women who are pregnant or who could become pregnant should not take Vinpocetine because it may cause miscarriage or harm fetal development, the FDA warned in a news release today.

Recalls & Warnings

April 21, 2020

U.S. Attorney's Office Bars Chiropractor from Selling Fake Coronavirus Cures

On April 17, 2020, the United States Attorney's Office for the Northern District of Texas announced that it has obtained a temporary restraining order preventing a chiropractor from promoting fake treatments for coronavirus (COVID-19). Dr. Ray L.

Recalls & Warnings

April 17, 2020

Joint Pain Supplement Isoprex Settles Charges of Making False Claims

On April 16, 2020, Renaissance Health Publishing, LLC, agreed to halt their allegedly deceptive advertising claims about their Isoprex supplement that targeted older consumers nationwide after the Federal Trade Commission (FTC) filed a complaint.

Recalls & Warnings

April 14, 2020

Teami Tea Settles Charges of Unproven Claims and Deceptive Celebrity Endorsements

On March 6, 2020, the FTC announced that Teami, LLC, a marketer of tea and skin care products, agreed to settle charges that it was selling products with unproven claims and misleading celebrity endorsements.

Recalls & Warnings

March 20, 2020

Seller of Rejuvenation Pills Settles Charges of Making False Claims

Health Center, Inc. has agreed to halt their allegedly deceptive advertising claims about three "cure-all" health and wellness products that targeted older consumers nationwide after the Federal Trade Commission (FTC) filed a complaint.

Recalls & Warnings

December 27, 2019

Federal Court Shuts Down Three Supplement Companies With Serious Manufacturing Violations

Update: (1/23/20) ABH has issued a recall of all its products, which are sold under various brand names by over 800 distributors and retailers. More details are available in CL's post about this recall.

Recalls & Warnings

December 05, 2019

Joint Supplement Synovia Was Promoted With Phony Testimonials, Says FTC

A.S. Research, LLC, has agreed to settle Federal Trade Commission (FTC) charges that they deceived consumers with false claims that their dietary supplement Synovia could treat arthritis and alleviate joint pain.

Recalls & Warnings

November 26, 2019

FDA Warns Companies Selling CBD Products as Dietary Supplements

On November 25, 2019, the FDA issued warning letters to 15 companies for selling products containing CBD (cannabidiol) labeled and marketed as dietary supplements, and/or for making drug claims about these products.

Recalls & Warnings

October 22, 2019

Seller of TrueAloe and AloeCran Settles Charges of Making False Claims

NatureCity, LLC, has agreed to settle Federal Trade Commission (FTC) charges that they deceived consumers by making false claims about their TrueAloe and AloeCran products.

Recalls & Warnings

July 18, 2017

Oat Cereal Recalled Due to Listeria Risk

On July 18, 2017, Garden of Light, Inc., recalled Woodstock Organic Matcha Vanilla Oats because of potential contamination with Listeria monocytogenes.

Recalls & Warnings

December 22, 2014

Nutrition Bars Recalled Due to Potential Salmonella Contamination

On December 19, 2014, Perfect Bar & Company issued a recall of certain lots of Peanut Butter and Cranberry Crunch Nutrition Bars because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

May 10, 2007

FDA Warns of Two Supplements Containing Pharmaceutical-like Compounds

On May 10, 2007, the FDA advised consumers not to purchase or use "True Man" or "Energy Max" products promoted and sold as dietary supplements throughout the United States.

Recalls & Warnings

December 02, 2014

Seller of Energy & Joint Supplements, Aloe, Silver and More Warned for Drug Claims

On November 24, 2014, the FDA issued a warning letter to Jansen Enterprises, LLC, dba HealthWorksUSA, following an inspection of the company's website which found statements made about Nutra Blast Natural Energy, Ionic Silver Water, Nutra Complete, and Nutra Gel to be drug claims. 

Recalls & Warnings

June 03, 2015

Maker of B-12 Energy Supplement Warned for Manufacturing Violations

On May 15, 2015, the FDA issued a warning letter to LiquidCapsule Manufacturing, LLC.

Recalls & Warnings

September 30, 2015

Weight and Energy Supplement Contains Synthetic "Amphetamine"

On September 21, 2015, the FDA issued a warning letter to TruVision Health LLC. because the company's supplement tru Weight & Energy lists a synthetic, amphetamine-like compound, AMP (also called 1,3-dimethylbutylamine or DMBA) on product labels. 

Recalls & Warnings

July 06, 2012

Centrum Multivitamins: Breast and Colon Health Claims Pulled

On July 5, 2012, Pfizer Consumer Healthcare announced it will withdraw breast and colon health claims from its Centrum multivitamin advertising and labels, and will revise health and energy claims made on other Centrum products.

Recalls & Warnings

November 25, 2007

Recall of Men's "Sexual Energy" Supplement Expanded to Include "Energy Max" Product

On November 16, 2007, American True Man Health Incorporated announced that it is expanding it's voluntary recall of the Company's dietary supplement product sold under the name and identified as True Man's Sexual Energy Nutriment Men's Formula with the expiration date up to and including December ...

Recalls & Warnings

April 18, 2013

Cardio, Energy and Sexual Enhancement Supplement Distributor Warned For Manufacturing Violations and Drug Claims

On December 21, 2012, the FDA issued a warning letter to ForMor Inc, dba ForMor International, following a facility inspection which found the company's Cardio Cocktail and Argenix dietary supplements to be adulterated because because they were prepared, packed, or held under conditions that do ...

Recalls & Warnings

June 09, 2016

Nature Made Multis and B Complex Recalled Due to Salmonella, Staph Risk

On June 8, 2016 Pharmavite LLC issued a recall of the following Nature Made® multivitamin and B complex supplements because they have the potential to be contaminated with Salmonella or Staphylococcus aureus:

Recalls & Warnings

June 26, 2006

FDA Warns Candy Maker Making Heart Health Claims

On May 31, 2006, the U.S.

Recalls & Warnings

December 06, 2013

Weight Loss Supplement Claims Challenged

On November 27, 2013, the National Advertising Division (NAD) recommended HealthyLife Sciences, LLC, modify or discontinue the use of certain claims made about the company's weight loss supplement Healthe Trim.

Recalls & Warnings

November 20, 2013

Another Meth-Like Compound Discovered In Weight Loss Supplements

A "non-natural" amphetamine-like compound, identified as beta-methylphenethylamine, was discovered in nine supplements recently tested by FDA scientists.

Recalls & Warnings

July 19, 2014

Powdered Caffeine Can Be Lethal, FDA Warns

On July 18, 2014, the FDA warned consumers to avoid powdered pure caffeine sold in bulk bags over the internet.

Recalls & Warnings

December 30, 2014

Maker of Aloe, Weight Loss Supplements and More Warned for Manufacturing Violations, Drug Claims

On December 17, 2014, the FDA issued a warning letter to Dandy Day Corporation, following a facility inspection which found the company's products, including Aloe Pearl, Alfalo, Aloespring, Crave Away, Original Supreme Energy, Ener "G," Can G, Flora G, Flora G Plus, and Garolic, to be adulterated ...

Recalls & Warnings

September 27, 2016

Seller of B Vitamins, Omega-3s and More Warned for Manufacturing Violations, Drug Claims

On September 15, 2016, the FDA issued a warning letter to Positive Power Nutrition, following a facility inspection which found the company's products, including High Energy C-Complex, Positive Vitality, Positive Performance, Positive CardioGuard, B-Complex 100, Positive Essentials, Positive ...

Recalls & Warnings

August 29, 2012

Herbal Supplement Company Warned For Medical Claims

On August 2, 2012, the FDA issued a warning to HSAC Enterprises, Inc. dba Kare-N-Herbs subsequent to a facility inspection and website review in May 2012 which found statements made about Kold Kare, Energy Kare and Tranquility Kare dietary supplements to constitute drug claims.

Recalls & Warnings

January 28, 2014

Emergen-C Settles False Advertising Lawsuit

Alacer Corp., marketers of Emergen-C, has agreed to pay $6.45 million to settle a class action lawsuit which charged the company made false claims that the vitamin C supplement could boost immunity, energy and metabolism.

Recalls & Warnings

June 29, 2018

Prescript-Assist Probiotic Recalled

On June 29, 2018, LL's Magnetic Clay, Inc., issued a recall of certain lots of Prescript-Assist, a "broad spectrum probiotic and prebiotic" supplement, because they may contain undeclared almonds, crustaceans, dairy, casein, eggs, and peanuts. 

Recalls & Warnings

November 01, 2013

Protein Shakes Containing Prescription Drug Pose Serious Health Risk

On November 1, 2013, Health Canada warned consumers that Vega One Vanilla Chai (sizes 437g and 874g) and Vega Sport Performance Chocolate nutritional shakes, by Sequel Naturals Ltd., have been found to contain the prescription antibiotic chloramphenicol.

Recalls & Warnings

July 30, 2014

Nutrition Bars Recalled Due to Salmonella Risk

On July 25, 2014, GoMacro issued a recall of two flavors of MACROBARS nutrition bars because they contain carob powder which has the potential to be contaminated with Salmonella.

Recalls & Warnings

September 26, 2014

FDA Warns Seller of Supplements and Chocolate Promoted to Treat Ebola

On September 23, 2014, the FDA issued a warning letter to Natural Solutions Foundation, following a review of the company's websites which found statements made about Silver Sol Nano Silver (also called The Silver Solution) and CBD Organic Dark Chocolate Bars (also called High Potency CBD Hemp Oil) ...

Recalls & Warnings

May 23, 2015

Colostrum Supplement Recalled

On May 14, 2015, the Natural Creations issued a recall of a small quantity of Natural Creations New Zealand Colostrum because the label does not state that the product is milk-based.

Recalls & Warnings

March 06, 2009

"The Truth About Nutrition" Marketers Agree to Pay $3 Million to Settle Charges of Deceptive Advertising of Dietary Supplements and Devices

On March 6, 2008, the Federal Trade Commission (FTC) announced that marketers of dietary supplements and health-related devices have agreed to pay $3 million in consumer redress to settle FTC charges that they deceptively claimed their products treated or prevented a wide variety of serious ...

Recalls & Warnings

August 09, 2012

FDA Warns Sports Nutrition Manufacturer of GMP Violations

On June 26, 2012, the FDA issued a warning letter to Parrillo Performance subsequent to a manufacturing and packing facility inspection which found Parrillo products to be adulterated due to current Good Manufacturing Practices (cGMP) violations.

Recalls & Warnings

December 29, 2015

Whey Protein Recalled

On December 23, 2015, American Pure Whey issued a recall of all lots of 100% Pure Whey Protein Matrix and 100% Pure Whey Protein Isolate because they contain undeclared milk and soy.

Recalls & Warnings

September 02, 2015

Antioxidant Supplement Recalled

On August 28, 2015, VRVK Nutraceuticals, LLC, DBA Dr. Venessa's Formulas, issued a voluntary recall of Ultimate Antioxidant Tablets because they may contain the undeclared allergens crustacean shellfish and milk.

Recalls & Warnings

May 23, 2016

Amino Acid Supplements Recalled

On May 18, 2016, Ultimate Nutrition Inc. issued a recall of its Amino Gold amino acid tablets and capsules because they contain undeclared milk in the form of hydrolyzed whey protein.

Recalls & Warnings

February 27, 2018

Testosterone, Thyroid, Other Supplements Recalled Due to Undeclared Milk

On February 23, 2018, Progressive Laboratories, Inc., issued a recall of the following four supplements because they may contain undeclared milk:

Recalls & Warnings

June 11, 2015

FDA Warns Maker of Fruit Energy Drinks for Drug Claims

On May 19, 2015, the FDA issued a warning letter to CK Management, Inc. following a facility inspection which found statements made on product labels and websites about Whole5, Fruit of the Spirit and ViaViente "whole food" fruit puree energy drinks to be drug claims.

Recalls & Warnings

February 24, 2015

Seller of Antioxidant Water, Energy Drops Warned for Manufacturing Violations and Drug Claims

On February 18, 2015, the FDA issued a warning letter to Better Health Lab, Inc.

Recalls & Warnings

March 09, 2012

Maker of Inhaled Caffeine Product Gets Warning

The U.S. FDA issued a Warning Letter to Breathable Foods, Inc. (dated March 5, 2012) advising that their product AeroShot, which is promoted for "breathable energy," is falsely labeled (misbranded).

Recalls & Warnings

January 23, 2013

USPLabs Settles Class Action Lawsuit Over Controversial DMAA Ingredient

On December 18, 2012, a settlement was approved in the class action lawsuit against USPLabs, which alleged the company's use of the ingredient DMAA (1,3-dimethylamine) in the supplements OxyELITEPRO and Jacked3d was not safe or legal.

Recalls & Warnings

September 05, 2013

Seller of Herbal Supplements and "Tonics" Warned For Manufacturing Violations and Drug Claims

On May 24, 2013, the FDA issued a warning letter to Sundial Herbal Products following a facility inspection which found the company's products, including Woman Back Tonic, Koromantee, Wood and Root Tonic, Arthritis, Asthma, Diabetics, Sundial Ashanti Weight Loss Energy Lifter, Appetite Suppresser, ...

Recalls & Warnings

January 23, 2015

Maker of Vitamin Drinks Warned for Manufacturing Violations

On January 7, 2015, the FDA issued a warning letter to NYSW Beverage Brands, Inc.

Recalls & Warnings

October 08, 2014

Consumers Who Have Purchased Red Bull May Qualify for Cash Payment or Free Red Bull Products

Consumers who purchased Red Bull products in the United States between January 1, 2002 and October 3, 2014 may be entitled to a $10 cash payment or two free Red Bull products, according to a proposed settlement of two class action lawsuits.

Recalls & Warnings

October 16, 2013

Methamphetamine-Like Compound Found In Popular Workout Supplement

A study published on October 14, 2013 (Cohen, Drug Test Analysis 2013) reports that the popular pre-workout energy supplement Craze (Driven Sports) has been found to contain the banned methamphetamine — like compound, N, á-diethylphenylethylamine.

Recalls & Warnings

March 15, 2016

FDA Warns Sellers of Weight and Workout Supplements Containing Acacia Rigidula

On March 7, 2016, the FDA issued warning letters to five sellers of supplements which were labeled as containing Acacia rigidula, an ingredient which is not permitted in dietary supplements.

Recalls & Warnings

October 17, 2015

23,000 ER Visits Linked to Supplements: Palpitations, Swallowing Problems, Allergies Common

Approximately 23,000 emergency room visits per year are attributed to adverse events linked to the use dietary supplements, according to a large, long-term study by the FDA and the Centers for Disease Control and Prevention (CDC).

Recalls & Warnings

March 17, 2015

Seller of Tea Warned for Drug Claims

On March 4, 2015, the FDA issued a warning letter to Four Elements Organic Herbals, LLC because statements made about HERBAL TEA Power, Energy & Stamina, ORGANIC HERBAL TEA Tulsi TelepaTea, ORGANIC HERBAL TEA To Your Health, Hawthorn Fresh Herb Extract, Elderberry Fresh Herb ...

Recalls & Warnings

November 27, 2018

High Levels of Lead Found in Kratom Products

Some kratom products contain levels of lead and nickel that are not considered safe for human consumption, according to tests conducted by the FDA.

Recalls & Warnings

April 16, 2019

DMHA and Phenibut Are Not Permitted in Dietary Supplements, Warns FDA

On April 16, 2019, the FDA announced it has issued 11 warning letters to companies whose dietary supplement products contain the drugs DMHA or phenibut, and therefore are in violation of the law.

Recalls & Warnings

July 10, 2018

Blissful Remedies Kratom Recalled Due to Salmonella Risk

On June 30, 2018, Blissful Remedies issued a recall of three kratom products because they have the potential to be contaminated with Salmonella.  

Recalls & Warnings

June 19, 2018

FDA Warns Seller of Weight Control Patches

On June 6, 2018, the FDA issued a warning letter to Health Management Group, Inc.

Recalls & Warnings

May 29, 2018

FDA Warns Seller of "Aromatase Inhibitor" Supplement

On May 18, 2018, the FDA issued a warning letter to Performance Nutrition Formulators LLC d.b.a. VMI Sports because its product Arimistane contains Androsta-3,5-Diene-7,17-Dione, an ingredient that the FDA considers to be a new drug and not a dietary supplement ingredient.

Recalls & Warnings

September 19, 2018

FDA Warns Seller of Shilajit

On September 6, 2018, the FDA issued a warning letter to Adaptive Energy LLC, following an inspection of the company's website, which found statements made about its shilajit product, Purblack were found to be drug claims.

Recalls & Warnings

September 09, 2018

Higenamine -- A Potentially Dangerous Stimulant -- Found in Some Supplements

A recent study found concerningly high doses of the stimulant higenamine in some weight loss, energy and sports supplements sold in the U.S. Higenamine is a naturally-occurring stimulant which is permitted to be sold as a dietary supplement ingredient in the U.S.

Recalls & Warnings

August 03, 2018

Vanilla Almond Breeze Almond Milk Recalled

On August 2, 2018, HP Hood LLC issued a recall of half-gallon (1.89 L) cartons of refridgerated Vanilla Almond Breeze almond milk because the product may contain milk, an allergen not listed on the label.

Recalls & Warnings

July 24, 2018

Contaminated Homeopathic Products Recalled

On July 20, 2018, King Bio issued a recall of four lots of its homeopathic products Aquaflora Candida HP9, Lymph Detox, and Baby Teething liquids because they were found to contain microbial contaminants including Pseudomonas Brenneri, Pseudomonas Fluroescens and ...

Recalls & Warnings

August 04, 2015

Whey, Casein and Colostrum Products Recalled

On August 3, 2015, Nutrition Resource Services, Inc. issued a voluntary recall of certain Just Be Natural (JBN) and Gifted Nutrition powders containing whey concentrate, whey isolate, casein, and colostrum because they contain undeclared milk.

Recalls & Warnings

February 16, 2016

Garden Of Life Recall Expanded

On February 13, 2016, Garden of Life LLC expanded its January 2016 recall of certain Raw Meal Organic Shake & Meal Chocolate, Original, Vanilla and Vanilla Chai products to include additional lots of these products, because they have the potential to be contaminated with ...

Recalls & Warnings

June 23, 2016

Protein Drinks Recalled Due to Possible Spoilage

On June 22, 2016 Bolthouse Farms issued a recall of the protein drinks listed below due to possible spoilage that may cause the beverages to appear lumpy, taste unpleasant and have an off odor.

Recalls & Warnings

June 18, 2016

Muscle Milk Protein Drinks Recalled

On June 17, 2016 HP Hood LLC issued a recall of the following Muscle Milk protein drinks because they have the potential for premature product spoilage:  

Recalls & Warnings

January 21, 2015

Smoothie Blends Recalled Due to Potential Listeria Contamination

On January 18, 2015, Inventure Foods, Inc. issued a recall of RADER FARMS Fresh Start Smoothie Blend, Fresh Start Sunrise Refresh Fusion, and Fresh Start Daily Power Fusion, because they have the potential to be contaminated with Listeria monocytogenes.

Recalls & Warnings

January 31, 2015

Protein Powder Recalled Due to Food Poisoning Risk

On January 30, 2015, Aloha, Inc. issued a voluntary recall of all packages of Premium Protein powder blends in chocolate and vanilla because they have the potential to be contaminated with Staphylococcus enterotoxin .

Recalls & Warnings

April 06, 2018

Workout Supplements Recalled Due To Allergen Risk

On April 5, 2018, Independent Nutrition Inc, dba Back to Health of Eugene., issued a recall of certain lots of Ignite High Endurance Pre-Workout Supplements because they may contain undeclared milk.

Recalls & Warnings

January 31, 2017

Vegetarian Protein Drink Recalled Due to Undeclared Milk

On January 28, 2017 NSE Products, Inc. (a subsidiary of Nu Skin Enterprises, Inc.) issued a recall of its vegetarian ageLOC TR90 Protein Boost protein drink because it contains undeclared milk.  

Recalls & Warnings

July 10, 2017

Bodybuilding Supplements Containing Steroid-Like Substances Recalled

On June 29, 2017, Hardcore Formulations recalled all lots and expiration dates of their products Ultra-Sten and D-Zine, bodybuilding supplements found to contain methylstenbolone and dymethazine, which are derivatives of anabolic steroids.

Recalls & Warnings

March 21, 2017

Plant-Based Protein Powders Recalled

On March 18, 2017 Nutiva issued a recall of three plant-based protein powder shakes after determining these products may contain peanuts.

Recalls & Warnings

May 11, 2006

Weight-Loss Marketers Pay $3 Million for Deceptive Advertising

On May 11, the Federal Trade Commission (FTC) announced that sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle charges that their deceptive claims violated federal law.

Recalls & Warnings

August 20, 2013

Weight Loss Supplement Formulas For Men and Women Recalled Due To Undeclared Drugs

On August 16, 2013, Herbal Give Care LLC issued a voluntary recall of all lots of weight loss dietary supplements Esbelder man, Esbelder fem and Esbelder siloutte because they were found to contain the undeclared drugs sibutramine, N-desmethylsibutramine, and N-di-desmethylsibutramine.

Recalls & Warnings

August 01, 2013

Fat Loss and Muscle Enhancement Supplements Found To Contain DMAA

On June 17, 2013, the FDA issued a warning letter to Formulife, Inc., dba Purus Labs, Inc., following a facility inspection which found the dietary supplements Fat Smack XR Thermolipolytic, Muscle Marinade Fresh Fruit and Muscle Marinade Cherry Limeade to contain DMAA.

Recalls & Warnings

July 26, 2013

Safety of Certain Weight Loss and Bodybuilding Supplements Called Into Question

On July 25, 2013, USA Today reported that several supplements, including weight loss, body building and sports nutrition supplements, have come under scrutiny after being found to contain illegal ingredients, or were associated with failed drug tests and adverse events.

Recalls & Warnings

February 13, 2013

Manufacturer of Heart, Multivitamin, Cranberry, and Longevity Supplements Warned For Adulteration and Drug Claims

On January 29, 2013, the FDA issued a warning letter to M.D.R. Fitness Corp. following a facility inspection which found violations of good manufacturing practices which cause the company's products to be adulterated. 

Recalls & Warnings

November 01, 2016

FDA Warns Consumers Not to Use Twelve Energy and Sexual Enhancement Supplements

The FDA recently warned consumers not to buy or use the following "energy" and sexual enhancement supplements, which are sold on various websites and in some retail stores, because they were found to contain undeclared drugs: 

Recalls & Warnings

February 01, 2016

Garden of Life Shakes and Meals Recalled Due to Salmonella Risk

On January 29, 2016, Garden of Life LLC issued a recall of certain Raw Meal Organic Shake & Meal Chocolate, Original, Vanilla and Vanilla Chai products because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

June 21, 2005

FTC Settles Claims with Marketers of FiberThin and Propolene

On June 20, 2005, the Federal Trade Commission (FTC) announced that the marketers of the dietary supplements FiberThin and Propolene have settled FTC charges that their misleading weight-loss claims violated federal laws.

Recalls & Warnings

August 31, 2009

Court Orders Marketers of Supreme Greens and Coral Calcium to Pay Nearly $70 Million for Consumer Refunds

On August 27, 2009, a federal district court ordered the marketers of two dietary supplements – "Supreme Greens" and "Coral Calcium" – who claimed the products would cure ailments ranging from cancer and Parkinson’s disease to heart disease and autoimmune diseases to pay nearly $70 million for ...

Recalls & Warnings

May 07, 2012

FDA Warns Doctor Promoting Own Supplements Online as Treatments

On April 18, 2012 the U.S. Food and Drug Administration (FDA) sent a Warning Letter to Jacob Teitelbaum, M.D. of Fatigued to Fantastic, LLC regarding the promotion that company's products on its website www.endfatigue.com.

Recalls & Warnings

April 04, 2012

Maker of Protein Drinks and Supplements Warned of Manufacturing Violations

The FDA published a Warning Letter to Protica, Inc., a maker of protein drinks and supplements, regarding violations of manufacturing regulations discovered during inspection of its facility in Whitehall, PA. Affected products include the foods Amped Up-2oz, Fireball-2oz, Healthy Shot-2.

Recalls & Warnings

October 25, 2013

Supplement Company Warned For Numerous Manufacturing Violations

On August 2, 2013, the FDA issued a warning letter to DNE Nutraceuticals, Inc., following a facility inspection which found the company's products to be adulterated because they were packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.

Recalls & Warnings

March 03, 2012

FDA Warns Vitaganic of Manufacturing Violations

On February 8, 2012, the U.S. FDA sent a Warning Letter to Vitaganic, Inc. regarding violations of Current Good Manufacturing Practic (CGMP) regulations for dietary supplements found during an inspection of it manufacturing facility in Sunnyvale, California in October 2011.

Recalls & Warnings

January 04, 2012

Seller of "HCG Drops" for Weight Loss Warned by FDA and FTC of Violations

On December 21, 2011, the U.S. FDA and FTC sent a joint Warning Letter to hCG Drops LLC regarding its marketing of Slim Diet Drops. According to the letter, the product is considered an unapproved drug because it is promoted for drug-like uses on the company's website, including the following:

Recalls & Warnings

December 19, 2013

Maker of Joint Health Supplements Warned for Manufacturing Violations

On December 4, 2013, the FDA issued a warning letter to PurQuality, LLC.

Recalls & Warnings

April 03, 2014

Maker of Green Coffee Bean Extract and Weight Loss Supplement Warned for Manufacturing Violations

On March 13, 2014, the FDA issued a warning letter to Libi Labs, Inc.

Recalls & Warnings

June 24, 2014

CELLFOOD Recalled in Canada

On June 23, 2014, Health Canada recalled CELLFOOD (Nu Science), a supplement promoted for improved energy, endurance and natural health, because it was found to be an unauthorized health product.

Recalls & Warnings

March 19, 2014

Maker of Herbal Capsules and Extracts Warned for Manufacturing Violations

On September 19, 2013, the FDA issued a warning letter to Herbalist and Alchemist, Inc.

Recalls & Warnings

May 02, 2016

Liquid Multi Recalled Due to Allergen Risk

On April 26, 2016, Schaffner Distributing Pronutri LLC. issued a recall of Re-VITA-lize Whole Food Liquid Vitamin (in tropical orange flavor) because it contains undeclared soy lecithin. 

Recalls & Warnings

April 27, 2016

Multivitamin Recalled Due to Undeclared Allergens

On April 19, 2016, Nuvi Global Corporation issued a recall of StemVitae 30oz liquid multivitamin because they contain the undeclared milk and soy lecithin. 

Recalls & Warnings

April 23, 2016

More Multis Recalled Due to Allergen Risk

On April 21, 2016, MagZuma Nutrition issued a recall of the following multivitamin supplements because they contain the undeclared allergens soy and milk:

Recalls & Warnings

April 23, 2016

Multivitamin Recalled Due To Allergen Risk

On April 19, 2016, Exceptional Health Products issued a recall of Angel Wings Daily Multi 120 Capsules because they contain the undeclared potential allergens soy and milk. 

Recalls & Warnings

June 18, 2016

Antioxidant Supplement Recalled Due to Allergen Risk

On June 17, 2016 GMJ Natural Products Inc. issued a recall of 32 fluid oz. jugs of Jugo Moringa Plus Antioxidant because they contain undeclared whey protein.

Recalls & Warnings

March 06, 2015

Most Milk Free of Drug Residue, FDA Study Shows

On March 5, 2015, the FDA announced that more than 99% of milk samples tested in the U.S. were found to be free of drug residues of concern.

Recalls & Warnings

July 11, 2017

Protein Powder Recalled Due to Allergen Risk

On July 7, 2017, Biohealth Nutrition recalled its Precision Blend Cookies & Cream because it contains undeclared wheat.

Recalls & Warnings

April 09, 2018

Muscle and Recovery Supplements Recalled Due to Undeclared Milk

On April 6, 2018, AdvoCare International issued a recall of two lots of Muscle Strength and four lots of Nighttime Recovery dietary supplements because they may contain undeclared milk.

Recalls & Warnings

May 10, 2013

Protein Extract Recalled for Undeclared Allergens

On May 6, 2013, Pure Herbs Ltd. issued a voluntary recall of Protein Extract because it contains undeclared milk and soy allergens.

Recalls & Warnings

December 17, 2008

Airborne Settles Over False Advertising -- $7 Million to States

On December 17, 2008, the Seattle Times reported that Airborne Health, makers of a top-selling product marketed as a cold prevention and treatment remedy, signed a $7 million settlement to settle false advertising claims leveled by 32 state attorneys general and the District of Columbia.

Recalls & Warnings

March 17, 2004

Marketers of “Focus Factor” and “V-Factor” Fined for Advertising Claims

On March 17 , 2004 the Federal Trade Commission (FTC) reported that the marketers of “Focus Factor,” a dietary supplement that purports to improve concentration, and “V-Factor,” a supplement that purports to enhance sexual performance, have agreed to settle charges that they made numerous ...

Recalls & Warnings

January 11, 2002

Canada Requests Recall of Certain Ephedra/Ephedrine Products

OTTAWA - January 10, 2002 - Health Canada is requesting a recall from the market of certain products containing Ephedra/ephedrine after a risk assessment concluded that these products pose a serious risk to health.

Recalls & Warnings

June 15, 2003

FTC Alleges "Heartbar" Made Deceptive Claims About Effectiveness

On June 12, 2003, the Federal Trade Commission (FTC) announced that Unither Pharma, Inc. and United Therapeutics Corporation have agreed to settle FTC charges that they made deceptive claims in advertising for their HeartBar product.

Recalls & Warnings

April 21, 2018

NxtGen Botanicals Maeng Da Kratom Recalled

On April 18, 2018, NGB Corp. of West Jordan, Utah issued a recall of NxtGen Botanicals Maeng Da Kratom labeled bottles of encapsulated product because they have the potential to be contaminated with Salmonella. To date, one illness has been reported to the FDA.

Recalls & Warnings

April 09, 2018

Kratom Powders and Capsules Recalled Due to Salmonella Risk

On April 5, 2018, Club 13 issued a recall of certain kratom powders and capsules because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

February 06, 2018

FDA Links 44 Deaths to Kratom

On February 6, 2018, FDA announced it is now aware of 44 deaths associated with the use of kratom, an herb often promoted for pain relief, energy and for treating opioid withdrawal symptoms. This is an increase from the 36 deaths associated with kratom that the agency reported in November 2017.

Recalls & Warnings

July 20, 2017

Jail Time for Seller of Spiked Supplements

On July 18, 2017, Derek Vest, the former president of Gentech Pharmaceutical located in Fort Meyers, Florida, was sentenced to 18 months in prison for introducing misbranded food into interstate commerce.

Recalls & Warnings

November 14, 2017

36 Deaths Associated With the Use of Kratom Products

On November 14, 2017, FDA Commissioner Scott Gottlieb, M.D. issued a statement on the dangers of using products containing kratom, an herb often promoted for pain relief, energy and for treating opioid withdrawal symptoms.

Recalls & Warnings

October 18, 2017

FDA Warns Seller of Arthritis, Blood Pressure, Diabetes Supplements For Making Drug Claims

On August 15, 2017, the FDA issued a warning letter to Years to Your Health, Inc., following an inspection of the company's website which found a number of their products to be misbranded, as they contained drug claims.

Recalls & Warnings

October 04, 2017

Police Officer Dies From Kratom Overdose, Herb Currently Legal in Most States

A police officer who worked in narcotics in Tupper Lake, New York, died this summer of an overdose of the herb kratom, according to a report from ABC News.

Recalls & Warnings

September 26, 2017

FDA Warns Seller of DHEA, Creatine, Chromium & More for Manufacturing Violations, Drug Claims

On August 25, 2017, the FDA issued a warning letter to Mega-Pro Nutrition, Inc., following inspections of the facility and website www.mega-pro.

Recalls & Warnings

August 29, 2017

FDA Warns Seller of Supplements for Allergies, Joint Pain, Bone Health, and More

On August 16, 2017, the FDA issued a warning letter to Total Nutrition, Inc.

Recalls & Warnings

May 26, 2017

"Allergy" Supplement Containing Ephedra Recalled

On February 7, 2017, MusclMasster, LLC (DBA The Green Herb) of Wheat Ridge, CO issued a recall of all bottles of Al-Er-G Capsules , a product promoted to help allergies, because they contain ephedra.

Recalls & Warnings

May 26, 2017

Herbal "Sexual Enhancement Coffee" Recalled, One Death Reported

On May 25, 2017, Caverflo.com issued a recall of Caverflo Natural Herbal Coffee, an "herbal" instant coffee promoted for sexual enhancement, because it was found to contain the drugs sildenafil and tadalafil. 

Recalls & Warnings

July 08, 2017

CDC Warns Against Placenta Pills After Infant Becomes Sick

An infant in Oregon whose mother began taking capsules of dried placenta three days after giving birth was diagnosed with late-onset group B Streptococcus agalactiae (GBS) bacteremia, a strep infection which was linked to the placenta pill, according to a recently published report from the ...

Recalls & Warnings

September 02, 2016

Kratom To Be Classified a Schedule I Controlled Substance

On August 30, 2016, the U.S. Drug Enforcement Agency (DEA) announced its intent to classify the active compounds (mitragynine and 7-hydroxymitragynine) in kratom as Schedule I controlled substances.  

Recalls & Warnings

August 05, 2016

U.S. Marshals Seize $150,00 Worth of Kratom

On August 4, 2016, the FDA announced that U.S. Marshals seized approximately $150,000 worth of dietary supplements labeled as containing kratom from Nature Therapeutics (dba Kratum Therapy). The action was taken at the request of the FDA.

Recalls & Warnings

February 09, 2017

Herbal Supplement Found to Contain Ephedra Alkaloids Recalled

On February 7, 2017, Kingsway Trading Inc. issued a recall of Xanthium & Siler Combo (Bi Yan Pian) Dietary Supplement because it contains ephedra alkaloids.

Recalls & Warnings

November 29, 2016

Bentonite Clay Promoted for "Detoxification" Contaminated With Lead

On June 17, 2016, the FDA issued a warning letter to Best Bentonite, following a facility inspection and laboratory analysis of product sample which found the company's Best Bentonite to be contaminated with lead.

Recalls & Warnings

November 25, 2016

DMAA Product Recalled

On November 23, 2016, NutriVitaShop (a dba of Naturecom Inc.) issued a recall of its DMAA net weight 500g because it may contain DMAA.

Recalls & Warnings

February 28, 2015

Drugs Found in Male Enhancement Supplements

On December 11, 2014, the FDA issued a warning letter to Biogenix USA, LLC, following a facility inspection which found the company's sexual enhancement products, HAM, CE6 and SARMZ to contain undeclared drugs, as well as drugs which were listed on the label but are not permitted ...

Recalls & Warnings

September 26, 2015

Seller of Muscle Supplements and More Warned for Manufacturing Violations

On August 14, 2015, the FDA issued a warning letter to Chaotic Labz, Inc.

Recalls & Warnings

September 05, 2015

Maker of Multivitamin and Fish Oil Warned for Manufacturing Violations

On July 22, 2015, the FDA issued a warning letter to Westar Nutritional Corp. dba Viva Life Science, Inc.

Recalls & Warnings

April 29, 2015

FDA Targets Weight Loss and Workout Supplements Listing Synthetic Stimulant DMBA

On April 24, 2015, the FDA issued warning letters to sellers of weight loss and workout supplements that list a synthetic, amphetamine-like compound called 1,3-dimethylbutylamine (DMBA) on product labels. 

Recalls & Warnings

April 08, 2015

Does Your Weight Loss or Sports Supplement Contain Synthetic Amphetamine?

A study published on April 7, 2015, reported that among 21 weight loss, sports and cognitive enhancement supplements labeled as containing the plant extract Acacia rigidula, more than half were found to contain a synthetic, amphetamine-like compound called beta- methylphenylethylamine ...

Recalls & Warnings

July 02, 2015

Maker of Arthritis Supplement Warned for Manufacturing Violations, Drug Claims

On June 17, 2015, the FDA issued a warning letter to Desert Stream, Inc.

Recalls & Warnings

June 17, 2015

Maker of Joint Supplement Warned for Manufacturing Violations

On May 29, 2015, the FDA issued a warning letter to Total Health Advanced Nutrition, Inc.

Recalls & Warnings

October 14, 2015

No Vinpocetine in Some Vinpocetine Supplements; Picamilon Labels Not Accurate

A recently published study of 23 supplements listing vinpocetine as an ingredient found six did not contain any vinpocetine. Among those that did contain vinpocetine, most did not list amounts on the label, but amounts found in suggested daily servings varied by almost 100-fold, from 0.

Recalls & Warnings

February 16, 2016

Work Out and Weight Supplements Contain Synthetic Amphetamine-Like Compound

On February 3, 2016, the FDA issued a warning letter to ATS Labs, LLC because labels for the company's work out and weight loss supplements CFI, Weapon-X Pre-Workout Extreme, and Lady Lean list a synthetic, amphetamine-like compound, 4-amino-2-methylpentane citrate (also called ...

Recalls & Warnings

April 16, 2016

Workout Supplement Containing Acacia Rigidula Recalled

On March 18, 2016, Nubreed Nutrition, Inc. issued a recall of all lots of its "pre-workout" supplement Undisputed which is labeled as containing Acacia rigidula, an ingredient which is not permitted in dietary supplements. 

Recalls & Warnings

April 05, 2016

Muscle Enhancement Supplement Recalled

On April 5, 2016, Invisiblu International LLC issued a recall of one lot of the muscle enhancement supplement Continuum Labs LGD-Xtreme because it contains LGD-4033 Ligandrol. The risks of this ingredient are not known.

Recalls & Warnings

January 12, 2016

Over $400,000 Worth of Kratom Supplements Seized by U.S. Marshals

On January 6, 2016, U.S. Marshals seized nearly 90,000 bottles of dietary supplements labeled as containing kratom (brand name RelaKzpro) valued at over $400,000, from Dordoniz Natural Products LLC in South Beloit, Illinois. The action was taken at the request of the FDA.

Recalls & Warnings

February 13, 2014

Maker of Cholesterol and Workout Supplements Warned For Manufacturing Violations, Drug Claims and Unapproved Ingredient

On January 31, 2014, the FDA issued a warning letter to Exclusive Supplements Inc.

Recalls & Warnings

March 21, 2014

Products Containing Kratom Recalled Following FDA Import Alert

On March 14, 2014, SNI National issued a voluntary recall of all kratom supplements, including kratom XL 4 Pack, Maeng Da Kratom 10 Pack, Max Kratom 20 Pack, and Bali Kratom 40 pack, following an FDA-issued import alert on all products containing this ingredient.

Recalls & Warnings

September 27, 2013

Company Warned For Distributing Weight Loss Supplement Containing DMAA, Drug Claims

On September 6, 2013, the FDA issued a warning letter to Pure Energy Products, Inc., following a facility inspection which found that the company distributes a weight loss supplement, called obestrim, which contains dimethylamylamine, or DMAA.

Recalls & Warnings

October 27, 2013

Ingredient In Workout Supplements May Be Unsafe, FDA Warns

On October 11, 2013, the FDA directed USP Labs, LLC to cease distribution of workout supplement OxyElite Pro and and muscle-building supplement VERSA-1, which are labeled as containing the ingredient aegeline, or N-[2-hydroxy-2(4-methoxyphenyl) ethyl]-3-phenyl-2-propenamide.

Recalls & Warnings

February 17, 2015

Seller of Muscle Supplements Containing Synthetic Steroids Warned

On February 9, 2015, the FDA issued a warning letter to A2Z Industries, LLC, following a facility inspection which found the company's muscle enhancing supplements, including HaloV and EPI2A3A to be labeled as containing synthetic steroids.

Recalls & Warnings

September 30, 2014

U.S. Marshals Seize $5 Million Worth of Kratom

On September 25, 2014, U.S. Marshals seized more than 25,000 pounds of raw kratom valued at over $5 million from Rosefield Management, Inc. in Van Nuys, California. The action was taken at the request of the FDA.

Recalls & Warnings

April 16, 2012

Protein Supplement Maker Fails FDA Audit -- Many Products Affected

The FDA sent a Warning Letter (dated April 2, 2012) to Theta Brothers Sports Nutrition, Inc. regarding numerous violations of good manufacturing practices at its Lakewood, New Jersey facility.

Recalls & Warnings

April 12, 2013

FDA Warns Consumers About The Dangers Of DMAA

On April 11, 2013, the FDA warned consumers about the dangers of dietary supplements containing the ingredient 1,3-dimethylamylamine (DMAA).

Recalls & Warnings

February 20, 2013

FDA Warns USPLabs For Adulteration and Drug Claims

On December 4, 2012 the FDA issued a warning letter to USPLabs, LLC following facility inspections which found the company's products, including dietary supplements Jacked3d, OxyElite Pro, Prime, and Super Cissus, to be adulterated because they were prepared, packed, or held under conditions that ...

Recalls & Warnings

May 23, 2013

Maker of Liver Detox and Insulin Supplements Warned For Drug Claims

On April 24, 2013, the FDA issued a warning letter to Glucorell, Inc.

Recalls & Warnings

May 17, 2013

Hoodia, Sexual Enhancement Supplements and More Found To Be Adulterated, Misbranded

On March 01, 2013, the FDA issued a warning letter to Desert Rose Manufacturing, Inc.

Recalls & Warnings

December 21, 2012

Weight Loss Supplement Containing Undeclared Drug Recalled

On December 19, 2012, P&J Trading issued a voluntary recall of SLIMDIA REVOLUTION after FDA testing found the dietary supplement contains undeclared sibutramine.

Recalls & Warnings

September 18, 2012

Men’s Sexual Enhancement Supplement Containing Prescription Drug Recalled

On September 12, 2012, Body Basics Inc. issued a voluntary nationwide recall of ACTRA-Sx 500 Dietary Supplement Capsules after independent laboratory testing confirmed the supplement contains the prescription drug sildenafil citrate.

Recalls & Warnings

September 09, 2014

Maker of Popular Green Coffee Bean Extract Settles FTC Charges of Unsupported Weight Loss Claims

Applied Food Sciences, Inc., maker of green coffee bean extract GCA, has agreed to pay $3.5 million to settle FTC charges that weight loss claims made about the extract were not supported by scientific evidence.

Recalls & Warnings

August 21, 2014

Seller of Joint Supplement Warned for Manufacturing Violations and Drug Claims

On July 17, 2014, the FDA issued a warning letter to Klein Laboratories, Inc.

Recalls & Warnings

June 28, 2014

Chia Seed Recall Expanded

On June 26, 2014, HEALTH MATTERS AMERICA INC.

Recalls & Warnings

January 27, 2015

Green Coffee Bean Supplement Marketer Settles FTC Charges of Deceptive Claims

On January 26, 2015, the FTC announced that Pure Health LLC, Genesis Today, and owner of both companies, Lindsey Duncan, will pay $9 million to settle charges of deceptive weight loss claims made about the companies' green coffee bean extract products.

Recalls & Warnings

January 13, 2015

Seller of Speech Disorder Supplement Agrees to Settle FTC Charges of Deceptive Claims

NourishLife, LLC, seller of supplements promoted for treating children's speech disorders, has agreed to pay $200,000 in order to settle FTC charges that claims made on the company's website and in brochures were deceptive and not supported by science.

Recalls & Warnings

January 31, 2014

Weight Loss Supplement Containing DMAA Recalled

On January 30, 2014, YoungYou International ("YoungYou") issued a voluntary recall of Mega Slim Herbal Appetite Management capsules because they were found to contain DMAA.

Recalls & Warnings

May 29, 2014

Chia Powders and Smoothies Recalled Due to Salmonella Risk

On May 28, 2014, Navitas Naturals issued a voluntary recall of products containing its organic sprouted chia seed powder because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

February 23, 2016

Flax Seed and Chia Powders Recalled

On February 20, 2016, HEALTH MATTERS AMERICA INC., issued a recall of specific lots of Organic Traditions Sprouted Flax Seed Powder and Organic Traditions Sprouted Chia & Flax Seed Powder because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

June 25, 2016

Cholesterol-Lowering Supplement Recalled Due To Allergen Risk

On June 23, 2016 Michael's Naturopathic Programs issued a recall of certain lots of its Cholesterol Metabolism Factors dietary supplements because they contain undeclared milk.

Recalls & Warnings

May 14, 2016

Xylitol in Supplements Poses Danger for Dogs

On May 12, 2016, the FDA warned consumers that xylitol, a popular sweetener found in chewable vitamins, chewing gum, breath mints, toothpaste and a variety of other products, is toxic to dogs.

Recalls & Warnings

June 07, 2016

Step 2 Weight Loss Supplement Recalled

On June 7, 2016, The Body Shot Bar issued a recall of all lots of weight loss supplement Step 2 60 gold capsule (350 mg per) capsules which were distributed between March 1 through May 6 2016 because they were found to contain undeclared sibutramine.

Recalls & Warnings

November 19, 2016

GNC Women's Multi Recalled Due to Undeclared Allergen

On November 16, 2016, Nutra Manufacturing, Inc. issued a recall of one lot of GNC Women's Ultra Mega Time Release multivitamin because it contains undeclared milk.

Recalls & Warnings

February 28, 2017

Multivitamin Recalled Due to Allergen Risk

On February 14, 2017, Licata Enterprises issued a recall of all lots of its Supreme One and Theravits 100 multiple vitamins because they contain fish liver oil but is labeled as containing "no common allergens.

Recalls & Warnings

October 07, 2017

Weight Loss Supplement Recalled

On October 5, 2017, Kiriko, LLC recalled recalled all lots of A1 Slim 30 capsules after FDA analysis found the products to contain sibutramine, phenolphthalein and N-Desmethyl sibutramine.

Recalls & Warnings

January 25, 2018

Bulletproof Collagen Protein Recalled

On January 25, 2018, Bulletproof 360, Inc issued a recall of its Bulletproof Collagen Protein supplement because it contains undeclared milk.

Recalls & Warnings

January 16, 2018

Marketers of CellAssure and Cognify Settle FTC Charges of Deceptive Cancer Claims

On January 11, 2018, the FTC announced that CellMark Biopharma, LLC and its CEO, Derek E.

Recalls & Warnings

January 10, 2018

Lithium Supplement Contaminated With E. Coli, Health Canada Warns

On December 1, 2018, Health Canada (the Canadian equivalent of the FDA) warned consumers that it found Smart Brain Formulations Serotonin Support, a lithium ororate supplement sold on the website Robert Lamberton Consulting, to be contaminated with E. choli (Escherichia coli).

Recalls & Warnings

April 24, 2018

Traditional Medicinals "Throat Coat" Lemon Echinacea Herbal Tea Recalled in Canada

On April 24, 2018, Health Canada (the Canadian equivalent of the FDA) advised consumers that one lot of Traditional Medicinals Throat Coat Lemon Echinacea herbal tea is being recalled in Canada because it has the potential to contaminated by Salmonella.

Recalls & Warnings

November 03, 2011

Hoodia Marketers Fined and Banned from Business

On November 3, 2011, the Federal Trade Commission (FTC) announced that it settled charges brought against three people and two companies for deceptively advertising a supposed weight-loss supplement ingredient -- hoodia.

Recalls & Warnings

August 27, 2013

Immune Supplement Recalled Due To Undeclared Milk

On August 23, 2013, Reaction Nutrition, LLC issued a voluntary recall of immune support supplement LIVE CLINICAL 90 CAPS because it contains undeclared milk.

Recalls & Warnings

February 06, 2013

Ingredient Supplier Warned For Meal Replacement Product Misbranding and Adulteration

On October 4, 2012, the FDA issued a warning letter to dietary supplement ingredient supplier Raw Deal, Inc.

Recalls & Warnings

April 29, 2013

Recall: Multivitamin Containing Undeclared Milk

On April 26, 2013, Saratoga Therapeutics, LLC issued a recall of ebA Multivitamin Supplement because it may contain undeclared milk. The label describes the supplement as free of milk components.

Recalls & Warnings

July 24, 2006

Marketers of Seasilver Ordered to Pay Almost $120 Million

On July 24, 2006, the Federal Trade Commission (FTC) announced that the marketers of Seasilver, an alleged phony cure-all, have been ordered to pay almost $120 million for failing to comply with an earlier order requiring them to pay $3 million in consumer redress.

Recalls & Warnings

April 22, 2008

Court Upholds Order for Seasilver Marketers to Pay $120 Million

On April 16, 2008, the Federal Trade Commission (FTC) announced that the U.S.

Recalls & Warnings

February 29, 2008

FTC Sues Sellers of Weight-Loss Pills for False Advertising

On February 8, 2008 the The Federal Trade Commission (FTC) charged a business operation with violating federal law by falsely claiming that its weight-loss pills cause users to lose weight without dieting or exercise.