Dietary supplement recalls

71 federal recalls in the last 12 months. Federal recalls for dietary supplements. Sourced from the FDA.

Recent recalls

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  • Yunker Energy & Health supplement recalled for Vitamin E mismatch

    Sato Pharmaceutical's Yunker Energy & Health Herbal Supplement with Vitamins does not contain the amount of Vitamin E stated on its label. The affected product was distributed nationwide through two domestic distributors. No injuries have been reported.

    FDAJun 10, 2026Yunker

  • Better Weather Fix Elixir recalled for undeclared kratom

    Better Weather Actives LLC is recalling all lots of Better Weather Fix Elixir 15 ml because the product may contain undeclared Mitragynine and Mitragynine Pseudoindoxyl, which are kratom alkaloids. These substances can cause serious effects including nausea, vomiting, rapid heart rate, hallucinations, and in severe cases, respiratory depression or loss of consciousness.

    SeriousFDAMay 28, 2026Better Weather Actives

  • Llorens vitamin B-complex recalled for black particulate matter

    Llorens Pharmaceuticals is recalling Vitamin B-Complex, Vitamin C & Folic Acid dietary supplement (8 FL Oz bottles, Lot B2025, expiration 08/27) because some bottles contain black particulate matter. The contamination was identified before causing reported injuries.

    ModerateFDAMay 27, 2026Llorens

  • Wellnov supplements recalled for possible C. botulinum risk

    Wellnov Supplements is recalling 14 products, including Joint Nourish, FulviLife Complex, Liposomal multivitamin drops, Liposomal Collagen Booster, Liposomal Kids Liquid Multivitamin Drops, and Liposomal D3, B12 and Sleep sprays. The products are made by VitaminAlly LLC in Chandler, Arizona, and were sold nationwide and in Puerto Rico. The FDA says manufacturing practices fell short in ways that could allow bacterial contamination and possible C. botulinum, and no illnesses have been reported.

    ModerateFDAMay 27, 2026Joint Nourish14 products

  • Liquid Blenz Sea Moss Tonic recalled for botulism risk

    Liquid Blenz Sea Moss Tonic 16 oz and 32 oz bottles may not have been processed adequately to prevent the growth of Clostridium botulinum, a bacteria that can cause serious illness. The product was distributed in New York and sold online.

    ModerateFDAMay 27, 2026Liquid Blenz13 products

  • Mogo Moringa Capsules recalled for Salmonella risk

    Mogo Moringa LLC is voluntarily recalling two specific lots of Mogo Moringa Oleifera Capsules due to a possible Salmonella contamination concern. The affected lots are Lot 15525AA (expires 06/2027) and Lot 00926AA (expires 01/2028). No Salmonella was detected in the company's own testing, but the recall is being issued as a precaution while the FDA continues its review.

    SeriousFDAMay 25, 2026Mogo

  • Better Weather Fix Elixir recalled for undeclared kratom

    XD Investments LLC recalled Better Weather Fix Elixir dietary supplements after FDA testing found they contain undeclared mitragynine and mitragynine pseudoindoxyl—potent kratom alkaloids not listed on the label. These substances can cause serious health effects including rapid heart rate, hallucinations, severe addiction, and in rare cases, fatal respiratory depression, especially when combined with other medications or drugs.

    SeriousFDAMay 9, 2026XD Investments

  • Vital Nutrients Aller-C recalled for undeclared egg, soy, hazelnut

    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.

    SeriousFDAApr 15, 2026Vital Nutrients

  • Boner Bears, Blue Bull, Red Bull recalled for hidden sildenafil

    Pure Vitamins and Natural Supplements is recalling three male enhancement pouch products, with 15 pouches per box: Boner Bears Honey, Blue Bull Extreme and Red Bull Extreme. FDA analysis found undeclared sildenafil and tadalafil, prescription drug ingredients that are not listed on the label. The products were distributed in New Jersey, and no injuries have been reported.

    SeriousFDAApr 15, 2026Boner Bears Honey3 products

  • Imu-Tek Colostrum-5 supplements recalled for possible under-processing

    Imu-Tek Animal Health is recalling two products: Imu-Tek Colostrum-5 120-capsule bottles and Imu-Tek Colostrum-5 powder bottles. The company says the product may not have been fully processed. No injuries have been reported.

    ModerateFDAApr 8, 2026Imu-Tek2 products

  • Divided Sunset collagen peptides recalled for undeclared egg and fish

    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.

    ModerateFDAApr 8, 2026Divided Sunset

  • SiluetaYa Tejocote Roots supplement recalled for yellow oleander

    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.

    SeriousFDAApr 1, 2026SiluetaYa

  • Kian Pee Wan capsules recalled for undeclared dexamethasone

    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.

    SeriousFDAMar 30, 2026Buy-herbal.com

  • Winder Laboratories fluoride multivitamin recalled for low vitamin D

    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.

    ModerateFDAMar 25, 2026Winder Laboratories

  • Shaman Botanicals White Vein tablets recalled for higher-than-labeled 7-OH

    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.

    SeriousFDAMar 25, 2026Shaman Botanicals

  • Rosabella Moringa capsules recalled for Salmonella risk

    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.

    SeriousFDAMar 18, 2026Rosabella

  • Mojo Max Fusion XXX recalled for undeclared sildenafil and tadalafil

    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.

    SeriousFDAMar 11, 2026Mohamed Hagar

  • Agebox iKids-Growth supplements recalled for undeclared ibutamoren

    The FDA says Agebox iKids-Growth capsules contain ibutamoren, an ingredient that is not listed on the label and is not approved for use in these products. The recall covers two products, both sold as 60-count bottles of Agebox iKids-Growth capsules: a Day Formula and a Night Formula. No injuries have been reported.

    ModerateFDAMar 4, 2026Agebox2 products

  • Pure Factors sleep supplement recalled for undeclared milk allergen

    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.

    ModerateFDAFeb 25, 2026Pure Factors

  • Why Not Natural Moringa Capsules recalled for Salmonella risk

    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.

    SeriousFDAFeb 25, 2026Why Not Natural

  • Aonic Complete supplement shots recalled for bacteria contamination

    TKS Co-pack Manufacturing is recalling 2 products: Aonic Complete Hers and Aonic Complete His, single-serving 34 ml liquid dietary supplement shots in plastic bottles. The recall was issued because the products may contain coliforms, E. coli, or Pseudomonas aeruginosa. The products were distributed to a customer in Utah, and no injuries have been reported.

    ModerateFDAFeb 18, 2026Aonic2 products

  • Imu-Tek Immuno-5 colostrum powder recalled for undeclared milk

    Imu-Tek Immuno-5 Colostrum Powder (7 oz) contains milk that is not listed on the label. This poses a serious risk to people and pets with milk allergies or sensitivity. The affected product is Lot #216 with an expiration date of 4/16/2027.

    ModerateFDAFeb 11, 2026Imu-Tek

  • Diva Fam Sea Moss Gel recalled for potential botulinum contamination

    Diva Fam Inc's Apple and Cinnamon Sea Moss Gel Superfood may be contaminated with Clostridium botulinum, a bacterium that produces a dangerous toxin. The affected 16 FL OZ glass jars were distributed nationwide through retail stores and online sales. No illnesses have been reported so far.

    SeriousFDAFeb 11, 2026Diva Fam14 products

  • OptiWize Collagen Plus recalled for manganese below label amount

    OptiWize Inc. recalled OptiWize Collagen Plus (320 count bottles) after testing found the manganese level was lower than stated on the label. The company discovered that labeled ingredient quantities did not match the actual amounts in the product.

    FDAFeb 11, 2026OptiWize

  • Rheumacare capsules recalled for lead found in product

    Rheumacare capsules manufactured by Virgo UAP Pharma in India were found to contain lead due to manufacturing defects. The affected product is a 30-count bottle with lot numbers CAM040 (expires 06/30/2029) or CAL079-N (expires 09/30/2028). Only 4 bottles were distributed to a customer in New York.

    SeriousFDAFeb 11, 2026Handelnine Global

  • Green Lumber Natural Fuel For Men recalled for containing tadalafil

    Green Lumber Natural Fuel For Men capsules were sold as a supplement but contain tadalafil, a prescription medication approved only for treating erectile dysfunction and certain heart conditions. The product was marketed and sold without FDA approval and without listing tadalafil on the label. Tadalafil can cause serious side effects, especially in people taking certain other medications or with certain health conditions.

    SeriousFDAFeb 11, 2026Green Lumber

  • Live it Up Super Greens powder recalled for Salmonella risk

    Superfoods is recalling two Live it Up Super Greens whole food supplement powders, one plain and one Natural Wild Berry flavor, both sold in 30-day supplies (8.5 oz). The products may be contaminated with Salmonella Typhimurium. They were distributed nationwide, including Puerto Rico, Guam, the Virgin Islands, and the United Kingdom, and no illnesses have been reported.

    SeriousFDAFeb 4, 2026Live it Up2 products

  • Qunol turmeric capsules recalled for mold contamination

    Qunol Extra Strength Turmeric Capsules (1000mg) in 60-count and 120-count bottles have been recalled due to mold contamination in raw materials used to make the product. The contamination was found in material lots produced in July. No injuries have been reported.

    ModerateFDAFeb 4, 2026Qunol

  • Gold Star Distribution foods recalled for potential rodent exposure

    Gold Star Distribution Inc. distributed multiple food products from a facility where rodents and rodent activity were found. The recall affects snack foods, candy, beverages, baby food, and many other items sold in Indiana, Minnesota, and North Dakota.

    ModerateFDAJan 28, 2026Gold Star Distribution

  • Herbs Forever Ayurvedic supplements recalled for undeclared wheat

    Herbs Forever is recalling two Ayurvedic herbal supplements, Gastro Care (800 mg extract, 90 vegetarian capsules) and Hingwastika Churna (100 g, 90 vegetarian capsules), because they may contain wheat that is not listed on the label. People with a wheat allergy or celiac disease could have a serious reaction. The products were sold mainly online across the United States, and no injuries have been reported.

    SeriousFDAJan 21, 2026HerbsForever2 products

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