Dietary supplement recalls
112 federal recalls in the last 12 months. Federal recalls for dietary supplements. Sourced from the FDA.
- 2026-08-27FDA-PRLipofitLipofit Extreme Fat Burner recalled for hidden prescription drug and toxic substance
Lipofit Extreme Fat Burner 2.0 (Lot 25M12F, expiration 09/2027) contains undeclared fluoxetine, a prescription antidepressant, in the daytime tablets and undeclared 2,4-dinitrophenol (DNP), a toxic pesticide, in the nighttime tablets. Neither ingredient is approved for use in dietary supplements, and DNP is not approved by the FDA for any use in humans.
- 2026-07-19FDA-PRRelay Peak Research LLCZen Principle Moringa Capsules recalled for Salmonella risk
Zen Principle Moringa Capsules dietary supplement may be contaminated with Salmonella due to contamination in the moringa leaf powder ingredient. The affected product is Lot A6FF4 with a Best By date of 11/2028, distributed nationwide from December 2025 through July 2026 primarily online. No illnesses have been reported.
- 2026-07-08FDA-FoodProvision Health Corp. dba PH LabsClass IIVista MAX dietary supplement recalled for undeclared Yellow#5
Vista MAX, a dietary supplement distributed by Vision of Health, contains Yellow#5 food dye that was not listed on the label. Yellow#5 can trigger allergic reactions in people sensitive to it. The affected product was distributed to local retail stores in California.
- 2026-07-08FDA-FoodProvision Health Corp. dba PH LabsClass IIProvision Health Ocular Plus recalled for undeclared Yellow#5
Ocular Plus, an eye health dietary supplement containing lutein and zeaxanthin, contains Yellow#5 food dye that was not listed on the label. Yellow#5 can trigger allergic reactions in sensitive individuals. About 7,000 units across three lot numbers were distributed to retail stores in California.
- 2026-07-08FDA-FoodMOGO Moringa LLCClass IMOGO Pure Moringa capsules recalled for Salmonella risk
MOGO Pure Moringa Oleifera capsules may be contaminated with Salmonella Typhimurium. The contamination was discovered during testing. Affected bottles were sold online through Amazon, eBay, Etsy, and mogomiranga.com.
- 2026-04-15FDA-FoodBlueroot Health, Inc.Class IIStop using Vital Nutrients Aller-C supplements
Blueroot Health, Inc. is recalling Vital Nutrients Aller-C vitamin supplements because they contain egg, soy, and hazelnut that are not listed on the label. This poses a serious risk to people with allergies to these ingredients. The recall affects 100-count and 200-count bottles distributed across the U.S.
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IStop using Red Bull Extreme Male Enhancement Supplement
Red Bull Extreme Male Enhancement Supplement pouches contain sildenafil, a prescription drug ingredient that was not listed on the label. Sildenafil can cause serious health problems, especially if you take other medications or have certain medical conditions. The affected product was distributed in New Jersey with batch number ORB524 and a May 2024 manufacturing date.
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IStop using Blue Bull Extreme supplement
Blue Bull Extreme Male Enhancement Supplement contains undeclared sildenafil, a prescription medication. The product was not labeled to indicate the presence of this drug. Sildenafil can cause serious health effects, especially if you take other medications or have certain medical conditions.
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IStop using Boner Bears Honey Male Enhancement
Pure Vitamins and Natural Supplements, LLC is recalling Boner Bears Honey Male Enhancement pouches because they contain hidden prescription medications—sildenafil and tadalafil—that are not listed on the label. These drugs can cause serious health problems, especially for people taking certain other medications or with heart conditions.
- 2026-04-08FDA-FoodImu-Tek Animal Health, IncorporatedClass IIStop using Imu-Tek Colostrum-5 Powder
Imu-Tek Colostrum-5 Powder (Lot #22, expiration 020528) may not have been processed adequately, which could allow harmful bacteria to survive. The affected product was distributed across 29 states. No illnesses have been reported so far.
- 2026-04-08FDA-FoodImu-Tek Animal Health, IncorporatedClass IIStop using Imu-Tek Colostrum-5 capsules
Imu-Tek Animal Health is recalling Colostrum-5 120-capsule bottles (Lot #013, expiration 092826) because the product may be under-processed, which can affect its safety. The affected bottles were distributed across 33 states.
- 2026-04-08FDA-FoodTG FOODS INCClass IIStop using Divided Sunset collagen peptides
Divided Sunset Multi Collagen Peptides (8 oz pouch) contain egg and fish ingredients but do not clearly label them as allergens on the package. The ingredient list mentions eggshell membrane collagen and marine collagen but fails to state "EGG" or identify the fish species as required by law. This poses a risk to people with egg or fish allergies.
- 2026-04-01FDA-FoodSiluetaya, LLCClass IStop using SiluetaYa Tejocote Roots supplement
SiluetaYa Mexican Tejocote Roots Supplement Pieces contain yellow oleander, a toxic plant that can cause serious illness. The affected product was sold online in Arizona, California, New Mexico, New York, Texas, and Utah. This is a Class I recall, the FDA's most serious category.
- 2026-04-01FDA-FoodAmerican Laboratories, LLCClass IIStop using American Laboratories Pepsin powder
American Laboratories is recalling Pepsin 1:3000 Powder (Item #FTI-G0193-00, Lot Code 00160041) because it may be contaminated with Salmonella. The affected powder was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported so far.
- 2026-04-01FDA-FoodAmerican Laboratories, LLCClass IIStop using American Laboratories pepsin powder
American Laboratories is recalling Pepsin 1:10,000 Powder (Item #FTI-G0193-00, Lot Code 00560021) due to potential Salmonella contamination. The affected product was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported.
- 2026-04-01FDA-FoodAmerican Laboratories, LLCClass IIStop using American Laboratories Pepsin powder
American Laboratories is recalling Pepsin Full Strength Powder (Item #5000545, Lot Code 29460025) due to potential Salmonella contamination. The affected product was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported.
- 2026-04-01FDA-FoodHerbal Creations USAClass IIBulk packaged Colustrum Powder. packaged with generic product label.
Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
- 2026-03-30FDA-PRAphreseller (Buy-herbal.com)Stop using Kian Pee Wan capsules immediately
Kian Pee Wan capsules, sold online as a dietary supplement for weight gain and appetite, contain two hidden prescription drugs: dexamethasone (a corticosteroid) and cyproheptadine (an antihistamine). These drugs were not listed on the label. Taking these undeclared drugs can cause serious health problems including infections, high blood sugar, psychiatric issues, and withdrawal symptoms if stopped abruptly.
- 2026-03-25FDA-FoodWinder Laboratories, LLCClass IIICheck Winder Laboratories multivitamin bottles
Winder Laboratories is recalling certain batches of their grape-flavored multivitamin with fluoride chewable tablets because they contain less vitamin D than stated on the label. The FDA discovered this during an inspection. The affected products are the 0.25 mg and 1 mg formulations with specific lot numbers and expiration dates in October and November 2025.
- 2026-03-25FDA-FoodShaman Botanicals, LLCClass IStop using Shaman Botanicals White Vein tablets
Shaman Botanicals is recalling White Vein Advanced Alkaloids chewable tablets because testing found the active ingredient (7-hydroxymitragynine) is present in higher amounts than stated on the label. The label says 7.5 mg per serving, but the actual content is greater. No injuries have been reported.
- 2026-03-18FDA-FoodAmbrosia Brands LLCClass IStop using Rosabella moringa capsules
Rosabella brand moringa dietary supplement capsules distributed by Ambrosia Brands LLC may be contaminated with Salmonella, a bacteria that can cause serious illness. The recall affects multiple lots with expiration dates ranging from March 2027 through November 2027. This product was sold nationwide and internationally.
- 2026-03-11FDA-DrugStuffbyNainaxClass IStop using MR. 7 SUPER 700000 capsules
MR. 7 SUPER 700000 capsules contain hidden prescription drugs—sildenafil and tadalafil—that are not listed on the label. These are serious medications that can interact with other drugs and cause health problems. The product was sold without FDA approval.
- 2026-03-11FDA-DrugMohamed HagarClass IStop using Mojo Max Fusion XXX capsules
Mojo Max Fusion XXX capsules contain hidden prescription drugs—sildenafil and tadalafil—that were not listed on the label. These are potent medications that can cause serious health problems, especially if you take other drugs or have certain heart or blood pressure conditions. The FDA has not approved this product for sale.
- 2026-03-11FDA-DrugANTHONY TRINH, 123Herbals LLCClass IStop using SILINTAN 25 pills immediately
SILINTAN 25 pills, sold in 25-count bottles, contain an undeclared ingredient called meloxicam, a prescription pain reliever. The FDA found this ingredient was not listed on the label and the product was not approved by the FDA. The recall affects all lots currently in use.
- 2026-03-04FDA-DrugAgeboxClass IIStop using Agebox iKids-Growth Night Formula
Agebox iKids-Growth Night Formula contains ibutamoren, a substance not listed on the label or approved by the FDA for this product. The affected 60-count bottles were sold online through Agebox.com and Amazon.com. No injuries have been reported.
- 2026-03-04FDA-DrugAgeboxClass IIStop using Agebox iKids-Growth capsules
Agebox iKids-Growth Day Formula capsules contain an undeclared drug ingredient called ibutamoren that was not approved by the FDA. The product was sold without proper FDA authorization. This affects 60-count bottles with lot numbers 23101201, 24080801, and 25020701.
- 2026-02-25FDA-FoodPure Solutions, Inc.Class IIStop using Pure Solutions sleep formula
Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset contain bovine colostrum, which is a milk product, but the label does not warn about the milk allergen. People with milk allergies could have a serious reaction if they use this product.
- 2026-02-25FDA-FoodArt Monkey LLC dba Why Not NaturalClass IStop using Why Not Natural Moringa Capsules
Why Not Natural Moringa Capsules (lot #A25G051, expiration 07/2028) may be contaminated with Salmonella, a bacteria that can cause serious illness. The affected capsules were distributed nationwide. No illnesses have been reported so far.
- 2026-02-18FDA-FoodTKS Co-pack Manufacturing, LLCClass IIStop using Aonic Complete His supplement
Aonic Complete His liquid dietary supplement shots may be contaminated with harmful bacteria including E. coli and Pseudomonas aeruginosa. The affected product was distributed in Utah. No illnesses have been reported so far.
- 2026-02-18FDA-FoodTKS Co-pack Manufacturing, LLCClass IIStop using Aonic Complete Hers supplement
Aonic Complete Hers, a liquid dietary supplement drink shot, may be contaminated with harmful bacteria including E. coli and Pseudomonas aeruginosa. The contamination affects specific lots distributed in Utah. No illnesses have been reported.
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