Dietary supplement recalls
206 federal recalls on file. Federal recalls for dietary supplements. Sourced from the FDA.
- 2026-08-07FDA-PRLexunder IncFood to Live green powders recalled for Salmonella risk
Lexunder Inc., doing business as Food To Live of Brooklyn, NY, is recalling Food to Live brand green powder products because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and
- 2026-07-19FDA-PRRelay Peak Research LLCZen Principle Moringa Capsules recalled for Salmonella risk
Relay Peak Research LLC (Zen Principle Naturals) of Incline Village, NV is voluntarily recalling its Zen Principle® brand Moringa Capsules dietary supplement because the product has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections i
- 2026-07-08FDA-FoodProvision Health Corp. dba PH LabsClass IIVista MAX dietary supplement recalled for undeclared Yellow#5
Dietary supplement product Vista MAX contains undeclared Yellow#5.
- 2026-07-08FDA-FoodProvision Health Corp. dba PH LabsClass IIProvision Health Ocular Plus recalled for undeclared Yellow#5
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
- 2026-07-08FDA-FoodMOGO Moringa LLCClass IMOGO Pure Moringa capsules recalled for Salmonella risk
Product may be contaminated with Salmonella Typhimurium
- 2026-04-15FDA-FoodBlueroot Health, Inc.Class IIStop using Vital Nutrients Aller-C supplements
Contains undeclared egg, soy, and hazelnut
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IStop using Red Bull Extreme Male Enhancement Supplement
FDA analysis revealed the presence of undeclared sildenafil
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IStop using Blue Bull Extreme supplement
FDA analysis revealed the presence of undeclared sildenafil
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IStop using Boner Bears Honey Male Enhancement
FDA analysis revealed the presence of undeclared sildenafil and Tadalafil
- 2026-04-08FDA-FoodImu-Tek Animal Health, IncorporatedClass IIStop using Imu-Tek Colostrum-5 Powder
Product is potentially under-processed.
- 2026-04-08FDA-FoodImu-Tek Animal Health, IncorporatedClass IIStop using Imu-Tek Colostrum-5 capsules
Product is potentially under-processed.
- 2026-04-08FDA-FoodTG FOODS INCClass IIStop using Divided Sunset collagen peptides
The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH parenthetically or via a Contains statement.
- 2026-04-01FDA-FoodSiluetaya, LLCClass IStop using SiluetaYa Tejocote Roots supplement
Product contains yellow oleander
- 2026-04-01FDA-FoodAmerican Laboratories, LLCClass IIStop using American Laboratories Pepsin powder
Potential Salmonella contamination.
- 2026-04-01FDA-FoodAmerican Laboratories, LLCClass IIStop using American Laboratories pepsin powder
Potential Salmonella contamination.
- 2026-04-01FDA-FoodAmerican Laboratories, LLCClass IIStop using American Laboratories Pepsin powder
Potential Salmonella contamination.
- 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
FOR IMMEDIATE RELEASE – 03/30/2026 - Flushing, New York, Aphreseller (Ebay seller ID), Buy-herbal.com is recalling all lots of Kian Pee Wan capsules to the consumer level. FDA analysis has found that the product contains the undeclared drug ingredients dexamethasone and cyproheptadine. Products cont
- 2026-03-25FDA-FoodWinder Laboratories, LLCClass IIICheck Winder Laboratories multivitamin bottles
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
- 2026-03-25FDA-FoodShaman Botanicals, LLCClass IStop using Shaman Botanicals White Vein tablets
A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.
- 2026-03-18FDA-FoodAmbrosia Brands LLCClass IStop using Rosabella moringa capsules
Product may be contaminated with Salmonella
- 2026-03-11FDA-DrugStuffbyNainaxClass IStop using MR. 7 SUPER 700000 capsules
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
- 2026-03-11FDA-DrugMohamed HagarClass IStop using Mojo Max Fusion XXX capsules
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
- 2026-03-11FDA-DrugANTHONY TRINH, 123Herbals LLCClass IStop using SILINTAN 25 pills immediately
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.
- 2026-03-04FDA-DrugAgeboxClass IIStop using Agebox iKids-Growth Night Formula
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
- 2026-03-04FDA-DrugAgeboxClass IIStop using Agebox iKids-Growth capsules
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
- 2026-02-25FDA-FoodPure Solutions, Inc.Class IIStop using Pure Solutions sleep formula
Label declares bovine colostrum but does not declare milk allergen.
- 2026-02-25FDA-FoodArt Monkey LLC dba Why Not NaturalClass IStop using Why Not Natural Moringa Capsules
Potential to be contaminated with Salmonella
- 2026-02-18FDA-FoodTKS Co-pack Manufacturing, LLCClass IIStop using Aonic Complete His supplement
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
- 2026-02-18FDA-FoodTKS Co-pack Manufacturing, LLCClass IIStop using Aonic Complete Hers supplement
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
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