Dietary supplement recalls

FDA analysis found undeclared sildenafil in Boner Bears Chocolate Syrup, which was sold to consumers through the firm's website. Sildenafil is not listed on the product label. No injuries have been reported.

Serious·FDA·Nov 3, 2026·Boner Bears

Vitality Works Inc. is recalling one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules (120 count) because it may be contaminated with Salmonella. The product was sold online at Amazon.com and at Whole Foods Market stores in several states and D.C. No illnesses have been reported.

Serious·FDA·Oct 30, 2026·Vitality Works

JXK Enterprises, Inc. is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, sold as a male enhancement product. FDA lab testing found sildenafil, the active ingredient in the prescription drug Viagra, which is not listed on the label. The product was sold nationwide online through www.elyxr.com.

Serious·FDA·Oct 28, 2026·Boner Bears

Tonight We Ride, LLC recalled all lots of Ultimate Forza Male Supplement capsules because they contain three undeclared active ingredients: sildenafil and tadalafil (prescription drugs sold as Viagra and Cialis) and dapoxetine (not approved by the FDA). These ingredients were found through third-party testing and pose health risks, especially for people taking nitrate medications or with heart conditions.

Serious·FDA·Oct 24, 2026·Tonight We Ride

Primal Herbs Volume, sold as a herbal supplement, contains sildenafil—a prescription medication—that is not listed on the label. FDA testing confirmed the presence of this undeclared ingredient. The product was sold online between July 2 and September 19, 2025.

Serious·FDA·Oct 21, 2026·Primal Herbs

Evexias Health Solutions Amino Ultra capsules are mislabeled and do not declare fish oil as an ingredient. This poses a risk to people with fish allergies. The recall affects 30 bottles distributed across multiple states.

Moderate·FDA·Oct 21, 2026·Evexias Health Solutions

Pacific Health Sciences' Babies' Magic Tea Baby Sleep Gripe Water contains elevated levels of alcohol, despite being labeled as alcohol-free. The product is marketed for infants as young as 2 weeks old. About 953 units with lot number 25122bw and expiration date 12/2028 were sold through Amazon and a customer website.

Serious·FDA·Oct 21, 2026·Babies' Magic Tea

A&P Creations is recalling two products that contain sildenafil and tadalafil, prescription ingredients not listed on the label. The products are X10 Natural Enhancement Supplement, distributed by Natur Fuel, and biQ-FEL, distributed by Biofel. About 1,283 retail units of X10 and 3,116 bottles of biQ-FEL were distributed nationwide. No injuries have been reported.

Serious·FDA·Oct 14, 2026·A&P Creations2 products

FDA testing found that one lot of Babies' Magic Tea Baby Sleep Gripe Water contains ethanol, methanol, and isopropanol that are not listed on the label. These alcohols can impair the central nervous system, especially in infants, and may cause drowsiness, nausea, vomiting, or more serious effects depending on how much is used.

Serious·FDA·Oct 6, 2026·Pacific Health Sciences

Leader Formulas recalled RAPTURE Preworkout powder after FDA testing found it contains DMAA, a banned stimulant ingredient. DMAA can raise blood pressure and cause heart problems, including heart attack, shortness of breath, and chest tightness.

Serious·FDA·Oct 6, 2026·Leader Formulas

Foods Alive organic moringa leaf powder in 8oz pouches may be contaminated with Salmonella. About 1,691 pouches were distributed nationwide and online. No illnesses have been reported so far.

Serious·FDA·Sep 23, 2026·Foods Alive

Global Mix Inc. is recalling Niwali Tejocote Capsules and Niwali Tejocote Pieces because FDA testing found the products actually contain yellow oleander (Thevetia peruviana), a highly toxic plant. All parts of yellow oleander contain cardiac glycosides that can cause severe or fatal effects including nausea, vomiting, heart rhythm changes, and organ damage.

Serious·FDA·Sep 21, 2026·Global Mix

Food to Live Organic SuperGrass Powder in 6 oz, 12 oz, 1 lb, and 4 lb containers has been recalled due to Salmonella contamination. The affected products were distributed across the United States and U.S. Virgin Islands. No illnesses have been reported.

Serious·FDA·Sep 9, 2026·Food to Live

SUPPLX.com's Business Pill and Branch Manager for Men dietary supplements contain yohimbine that is not listed on the labels. FDA testing found dangerously high levels of this substance, which can cause serious heart problems, severe high blood pressure, and other dangerous side effects—especially in people taking stimulants or certain medications.

Serious·FDA·Sep 3, 2026·Supplx.com

Byron White Formulas is recalling three herbal supplements sold as A-L Complex, A-P, and A-FNG, all in 1.0 fl. oz. (30 mL) bottles. The English labels do not list walnuts, which are in the product, so people with a walnut allergy may not know it is there. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Byron White Formulas3 products

ZMB Enterprises' Addall XR Shot 1 liquid dietary supplement contains three undeclared ingredients that are banned or restricted by the FDA: 1,4-DMAA, Phenylethylamine, and Phenibut. The product was sold online between July and December 2025.

Serious·FDA·Sep 2, 2026·Addall XR

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.

Serious·FDA·Aug 27, 2026·Lipofit

Buy-Herbal's Kian Pee Wan Capsules contain two prescription drug ingredients—dexamethasone and cyproheptadine—that are not listed on the label and were not approved by the FDA. The product was sold online through eBay. No injuries have been reported.

Serious·FDA·Aug 19, 2026·Buy-Herbal

Zen Principle Naturals Moringa Leaf Powder dietary supplement capsules may be contaminated with Salmonella. The affected product is sold in 180-capsule and 360-capsule bottles. No illnesses have been reported so far.

Serious·FDA·Aug 12, 2026·Zen Principle Naturals

Ashfiat Alharamain Energy Support 250ml/8fl. oz. drinks contain undeclared tadalafil, a prescription medication used to treat erectile dysfunction. Tadalafil can cause serious health problems, especially when combined with certain other medications or in people with heart conditions. The affected product was sold nationwide through Amazon.com.

Serious·FDA·Aug 12, 2026·Ashfiat Alharamain

Mellish Island Super Skin capsules contain marine collagen derived from fish, but the product label does not declare this fish ingredient. People with fish allergies who consume this supplement without knowing it contains fish could have an allergic reaction.

Moderate·FDA·Aug 5, 2026·Mellish Island

TNVitamins 100% Organic Moringa Capsules (1,200 mg) and Moringa Powder (96 grams) have been found to be contaminated with Salmonella. The contamination affects specific lot numbers: Capsules (Lot #2800, expires 2/2028) and Powder (Lot #2782, expires 5/2028). No illnesses have been reported to date.

Serious·FDA·Jul 29, 2026·TNVitamins

Modern Warrior Ready, a dietary supplement sold in 60-capsule bottles, contains unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam. The FDA identified these ingredients through analysis. The product was distributed nationwide from April 2022 through December 8, 2025.

Serious·FDA·Jul 29, 2026·Modern Warrior

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.

Serious·FDA·Jul 19, 2026·Relay Peak Research LLC

Trafa Pharmaceuticals Inc. is recalling its organic moringa leaf powder (15 kg bags, batch #TRF-2025050801, manufactured May 8, 2025) due to potential Salmonella contamination. The affected product was distributed in New York.

Serious·FDA·Jul 15, 2026·Trafa Pharmaceuticals

PH Labs is recalling two dietary supplements, Ocular Plus and Vista MAX, because they contain Yellow No. 5 dye that is not listed on the label. Ocular Plus was distributed by L.A. Farmacia Natural and Vista MAX by Vision of Health, with about 6,967 units of each affected. The products went to two local retail stores, and no injuries have been reported.

Moderate·FDA·Jul 8, 2026·PH Labs2 products

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.

Serious·FDA·Jul 8, 2026·MOGO

Dkiru LLC's Adndale Magnesium Glycinate Gummies 400 mg contain melatonin that is not listed on the label. The affected product is sold in 90-count plastic bottles (UPC 860008784551) with three affected lot numbers expiring between August and September 2026. Melatonin is a sleep aid not declared in the ingredient list, which poses a risk to consumers who may not expect it or who should avoid it due to other medications or health conditions.

Moderate·FDA·Jun 24, 2026·Adndale

Total Nutrition Inc is recalling TNVitamins and Doctor's Pride brand moringa capsule supplements because they may be contaminated with Salmonella. The recall affects 13,000 bottles sold nationwide across multiple lot numbers.

Serious·FDA·Jun 17, 2026·TNVitamins

Sensory Supplement LLC is recalling Neuro Nourish dietary supplement due to premature lipid oxidation that can cause an off odor and bitter taste. The affected product is a 5.9 oz multi-nutrient supplement sold online nationwide. No injuries have been reported.

FDA·Jun 17, 2026·Neuro Nourish2 products