Some links on this site are paid links: if you buy through them, we earn a commission at no extra cost to you. This page has no paid links. Affiliate disclosure.
This page lists the dietary supplement recalls that the U.S. Food and Drug Administration (FDA) posted in its Enforcement Reports since November 8, 2024, newest first: 90 recalls. Our software downloads the list from the FDA’s public data service, openFDA, and rebuilds this page when the list changes. No AI writes or changes this page.
Check a supplement name
The suggestions come from the recalls listed on this page and from the supplement launches we reviewed.
At a glance
- 44 supplement recalls reported in the last 12 months: 17 Class I, 25 Class II, 2 Class III.
- Why they were recalled (last 12 months): 15 for hidden drug ingredients or banned stimulants, 11 for contamination (bacteria, metals or foreign material), 9 for undeclared allergens, 9 for labeling, quality or other problems.
- Still ongoing: 36 of the 90 recalls listed here (the FDA marks the others completed or terminated).
Supplement recalls, newest first
| Reported | Product | Reason | Class | Status |
|---|---|---|---|---|
| October 28, 2026 | PRIMAL HERBS Recalled by PRIMAL SUPPLEMENTS GROUP LLC Recall H-0172-2027 | FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label. | Class I | Ongoing |
| October 28, 2026 | Evexias Health Solutions Amino Ultra Recalled by EVEXIAS HEALTH SOLUTION Recall H-0170-2027 | The product is mislabeled and fails to declare fish oil. | Class II | Ongoing |
| October 28, 2026 | Babies' Magic Tea Recalled by Pacific Health Sciences Llc Recall H-0168-2027 | Adulterated (elevated levels of alcohol) infant dietary supplement | Class II | Ongoing |
| October 14, 2026 | X10 Natural Enhancement Supplement Recalled by A&P CREATIONS Recall H-0016-2027 | Product contains undeclared Sildenafil and Tadalafil. | Class I | Ongoing |
| September 2, 2026 | Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron… Recalled by Byron White Formulas, Inc. Recall H-1278-2026 | Label does not declare walnuts in English | Class II | Ongoing |
| September 2, 2026 | Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron… Recalled by Byron White Formulas, Inc. Recall H-1277-2026 | Label does not declare walnuts in English | Class II | Ongoing |
| September 2, 2026 | Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull)… Recalled by Byron White Formulas, Inc. Recall H-1276-2026 | Label does not declare walnuts in English | Class II | Ongoing |
| September 2, 2026 | Addall XR Shot 1 single bottle Recalled by ZMB Enterprises Recall H-1263-2026 | The product contains 1,4-DMAA, Phenylethylamine and Phenibut. | Class I | Ongoing |
| August 12, 2026 | Zen Principle Naturals Moringa Leaf Powder dietary supplement Recalled by FACTORY6, INC. Recall H-1222-2026 | Possible Salmonella in Moringa Leaf Powder product. | Class I | Ongoing |
| August 5, 2026 | Mellish Island Super Skin Recalled by Mellish Island Corp Recall H-1190-2026 | Firm's finished product label does not declare the source of marine collagen which was determined to be fish. | Class II | Ongoing |
| July 29, 2026 | Modern Warrior Ready Recalled by Modern Warrior Life, LLC Recall H-1178-2026 | FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam. | Class I | Ongoing |
| July 8, 2026 | Vista MAX Recalled by Provision Health Corp. dba PH Labs Recall H-1135-2026 | Dietary supplement product Vista MAX contains undeclared Yellow#5. | Class II | Ongoing |
| July 8, 2026 | Ocular Plus with Lutein Recalled by Provision Health Corp. dba PH Labs Recall H-1134-2026 | Dietary supplement product Ocular Plus contains undeclared Yellow#5. | Class II | Ongoing |
| July 8, 2026 | MOGO PURE MORINGA OLEIFERA CAPSULES Recalled by MOGO Moringa LLC Recall H-1128-2026 | Product may be contaminated with Salmonella Typhimurium | Class I | Ongoing |
| June 17, 2026 | NEURO NOURISH dietary supplement Recalled by SENSORY SUPPLEMENT LLC Recall H-1109-2026 | Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste. | Class II | Ongoing |
| June 10, 2026 | Yunker(branded) Energy & Health Herbal Supplement with Vitamins Recalled by Sato Pharmaceutical Inc. Recall H-0892-2026 | Product does not meet label claim for Vitamin E. | Class III | Ongoing |
| May 27, 2026 | Vitamin B-Complex Recalled by Llorens Pharmaceuticals International Division, Inc. Recall H-0809-2026 | Foreign object: black particulate matter | Class II | Ongoing |
| May 27, 2026 | Vitamin B-Complex Recalled by Safecor Health, LLC Recall D-0549-2026 | Presence of a Foreign Substance; black particles observed in liquid | Class II | Ongoing |
| April 15, 2026 | Red Bull Extreme Male Enhancement Supplement Recalled by Pure Vitamins and Natural Supplements, LLC Recall H-0655-2026 | FDA analysis revealed the presence of undeclared sildenafil | Class I | Ongoing |
| April 15, 2026 | Blue Bull Extreme Male Enhancement Supplement Recalled by Pure Vitamins and Natural Supplements, LLC Recall H-0654-2026 | FDA analysis revealed the presence of undeclared sildenafil | Class I | Ongoing |
| April 1, 2026 | SiluetaYa Mexican Tejocote Roots Supplement Pieces Recalled by Siluetaya, LLC Recall H-0647-2026 | Product contains yellow oleander | Class I | Ongoing |
| March 25, 2026 | Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine… Recalled by Shaman Botanicals, LLC Recall H-1108-2026 | A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification. | Class I | Ongoing |
| March 25, 2026 | Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine… Recalled by Shaman Botanicals, LLC Recall H-1107-2026 | A sample of the product had the active ingredient in a quantity greater than the labeled specification. | Class I | Ongoing |
| March 18, 2026 | Rosabella brand MORINGA Recalled by Ambrosia Brands LLC Recall H-0546-2026 | Product may be contaminated with Salmonella | Class I | Terminated |
| February 25, 2026 | Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset Recalled by Pure Solutions, Inc. Recall H-0537-2026 | Label declares bovine colostrum but does not declare milk allergen. | Class II | Ongoing |
| February 18, 2026 | Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot Recalled by TKS Co-pack Manufacturing, LLC Recall H-0521-2026 | Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. | Class II | Completed |
| February 18, 2026 | Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot Recalled by TKS Co-pack Manufacturing, LLC Recall H-0520-2026 | Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. | Class II | Completed |
| February 11, 2026 | Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use… Recalled by Imu-Tek Animal Health, Incorporated Recall H-0483-2026 | Undeclared milk allergen | Class II | Terminated |
| February 4, 2026 | a.) Live it Up brand Super Greens Recalled by SUPERFOODS, INC. Recall H-0434-2026 | Products may be contaminated with Salmonella Typhimurium | Class I | Completed |
| February 4, 2026 | Live it Up brand Super Greens Recalled by SUPERFOODS, INC. Recall H-0433-2026 | Products may be contaminated with Salmonella Typhimurium | Class I | Completed |
| January 21, 2026 | HerbsForever- Hingwastika Churna Recalled by Herbs Forever Recall H-0405-2026 | Potential undeclared allergen ingredient (Wheat) | Class I | Terminated |
| January 21, 2026 | HerbsForever- Gastro Care Recalled by Herbs Forever Recall H-0404-2026 | Potential undeclared allergen ingredient (Wheat) | Class I | Terminated |
| December 31, 2025 | Sinus Cap Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0348-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 31, 2025 | Pain Away Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0347-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 31, 2025 | Organic Ginger Root Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0346-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 31, 2025 | Ear Drops Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0345-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 31, 2025 | Chaga Mushroom Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0344-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 31, 2025 | Boswellia Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0343-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 31, 2025 | Baby Soothe Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0342-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 31, 2025 | Baby Allergy Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0341-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 31, 2025 | Anti-virus Herbal Supplement Recalled by A New Life Herbs, LLC Recall H-0340-2026 | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class II | Terminated |
| December 10, 2025 | Prenate Chewable¿ A chewable Rx prenatal vitamin with a delicious chocolate flavor with Quatrefolic… Recalled by Avion Pharmaceuticals, LLC Recall H-0233-2026 | Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per serving instead of 250mcg per serving. | Class III | Ongoing |
| December 10, 2025 | My Bladder Recalled by Water Pure, Inc. Recall H-0213-2026 | Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303 | Class II | Terminated |
| December 3, 2025 | Member's Mark Super Greens Dietary Supplement Recalled by MeriCal, LLC Recall H-0205-2026 | Potential contamination of Salmonella Richmond | Class I | Ongoing |
| October 15, 2025 | FemiClear Daily Bladder Strength Dietary Supplement Recalled by Organicare Nature's Science, LLC Recall H-0031-2026 | Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303. | Class II | Terminated |
| October 15, 2025 | Organic BABY bedtime drops Recalled by M.O.M Enterprises, LLC. Recall H-0025-2026 | Potential yeast contamination. | Class II | Ongoing |
| October 8, 2025 | vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black Girl… Recalled by Vitalabs, Inc. Recall H-0037-2026 | Undeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts. | Class II | Completed |
| October 1, 2025 | Mai Tai 20mg Gummies Brand Name: None Recalled by Extract Labs, Inc. Recall H-0624-2025 | Potential peanut protein cross-contact. | Class II | Terminated |
| October 1, 2025 | Blue Razz 20mg Gummies Brand Name: None Recalled by Extract Labs, Inc. Recall H-0623-2025 | Potential peanut protein cross-contact. | Class II | Terminated |
| October 1, 2025 | Elderberry 20mg Gummies Brand Name: None Recalled by Extract Labs, Inc. Recall H-0622-2025 | Potential peanut protein cross-contact. | Class II | Terminated |
| October 1, 2025 | Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg… Recalled by Extract Labs, Inc. Recall H-0621-2025 | Potential peanut protein cross-contact. | Class II | Terminated |
| September 24, 2025 | PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0601-2025 | Unapproved Drug Claims and Misbranded. | Class III | Terminated |
| September 24, 2025 | PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0600-2025 | Unapproved Drug Claims and Misbranded. | Class III | Terminated |
| September 24, 2025 | Top Secret Nutrition extra strength uric control fast acting multi-pronged uric acid control 30 veggie… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0599-2025 | Unapproved Drug Claims. | Class III | Terminated |
| September 24, 2025 | PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 SERVINGS SUPPORTS ENERGY PRODUCTION PROTEN… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0598-2025 | Unapproved Drug Claims and Misbranded. | Class III | Terminated |
| September 24, 2025 | PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0597-2025 | Unapproved Drug Claims and Misbranded. | Class III | Terminated |
| September 24, 2025 | LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH PCT LEGAL GEAR DIETARY SUPPLEMENT… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0596-2025 | Unapproved Drug Claims. | Class III | Terminated |
| September 24, 2025 | IFN iFORCE NUTRITION JOINT HELP HEALTHY JOINTS & LIGAMENTS DIETARY SUPPLEMENT 120 CAPSULES UPC 8 54503… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0595-2025 | Unapproved Drug Claims. | Class III | Terminated |
| September 24, 2025 | HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS RESPIRATORY HEALTH SUPPORTS… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0594-2025 | Unapproved Drug Claims and Misbranded. | Class III | Terminated |
| September 24, 2025 | HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP-1)… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0593-2025 | Unapproved Drug Claims and Misbranded. | Class III | Terminated |
| September 24, 2025 | HI-TECH PHARMACEUTICALS PINE BARK SUPPORTS HEART HEALTH & CIRCULATION SUPPORTS CARDIOVASCULAR HEALTH… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0592-2025 | Unapproved Drug Claims and Misbranded. | Class III | Terminated |
| September 24, 2025 | HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0591-2025 | Unapproved Drug Claims. | Class III | Terminated |
| September 24, 2025 | HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain… Recalled by Hi-Tech Pharmaceuticals Inc. Recall H-0590-2025 | Unapproved Drug Claims. | Class III | Terminated |
| September 17, 2025 | Organic BABY bedtime drops Recalled by M.O.M Enterprises, LLC. Recall H-0576-2025 | Potential for spoilage due to yeast contamination. | Class II | Ongoing |
| September 17, 2025 | Anabolic Research WINN-50 (vanazolol). Dietary Supplement. 90 Capsules. UPC 8 51840-00707 6. Manafactured… Recalled by Dynamic Sports Nutrition Recall H-0573-2025 | Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims. | Class III | Terminated |
| August 20, 2025 | Lithium Orotate Recalled by GMP Laboratories of America Inc Recall H-0448-2025 | Downstream recall of a dietary supplement ingredient that was manufactured out of specification. | Class III | Terminated |
| August 20, 2025 | Lithium Orotate 2.5 Recalled by GMP Laboratories of America Inc Recall H-0447-2025 | Downstream recall of a dietary supplement ingredient that was manufactured out of specifications. | Class III | Terminated |
| July 2, 2025 | Rodex Forte Recalled by Preventics, Inc. dba Legere Pharmaceuticals Recall H-0096-2025 | Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules. | Class III | Terminated |
| July 2, 2025 | NutriLean Recalled by Preventics, Inc. dba Legere Pharmaceuticals Recall H-0095-2025 | Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules. | Class III | Terminated |
| July 2, 2025 | Probese Caps Recalled by Preventics, Inc. dba Legere Pharmaceuticals Recall H-0094-2025 | Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules. | Class III | Terminated |
| July 2, 2025 | Protrim Plus Recalled by Preventics, Inc. dba Legere Pharmaceuticals Recall H-0093-2025 | Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules. | Class III | Terminated |
| July 2, 2025 | Super ProTHIN Plus Recalled by Preventics, Inc. dba Legere Pharmaceuticals Recall H-0092-2025 | Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules. | Class III | Terminated |
| July 2, 2025 | Prothin, dietary supplement. Seven Packets containing 2 tablets and 4 capsules. Legere Pharmaceuticals… Recalled by Preventics, Inc. dba Legere Pharmaceuticals Recall H-0091-2025 | Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules. | Class III | Terminated |
| June 18, 2025 | ULTRA ARMOR Recalled by SAINI TRADE INC Recall D-0466-2025 | Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil. | Class I | Ongoing |
| June 18, 2025 | ELECTRO BUZZ Recalled by SAINI TRADE INC Recall D-0465-2025 | Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil. | Class I | Ongoing |
| June 18, 2025 | MALEXTRA Recalled by SAINI TRADE INC Recall D-0464-2025 | Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil. | Class I | Ongoing |
| June 18, 2025 | Male Ultra Recalled by SAINI TRADE INC Recall D-0463-2025 | Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil. | Class I | Ongoing |
| June 11, 2025 | Nordic Naturals Zero Sugar Kids Multivitamin Supplement Recalled by Nordic Naturals, Inc. Recall F-0840-2025 | Product is mislabeled. | Class III | Terminated |
| June 4, 2025 | ENDURANCE BOOST WITH HORNY GOAT WEED Recalled by EnShiShiXiangNiShangMaoYouXianGongSi Recall D-0453-2025 | Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue). | Class I | Ongoing |
| April 30, 2025 | Spermidine Recalled by Supplement Manufacturing Partner Inc. Recall F-0729-2025 | Undeclared allergen: Wheat | Class I | Terminated |
| April 16, 2025 | MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement Recalled by MTN OPS, LLC Recall F-0698-2025 | Undeclared soy flour | Class II | Terminated |
| April 9, 2025 | Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml Recalled by Bioriginal Food & Science Corporation Recall F-0709-2025 | Undeclared allergens: Soy lecithin | Class II | Terminated |
| April 2, 2025 | Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES Recalled by Veridance Pharmacal, LLC Recall F-0671-2025 | Levels of iodine exceeding label claim | Class II | Terminated |
| March 26, 2025 | Vitality Recalled by One Source Nutrition, Inc, Recall D-0281-2025 | Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared sildenafil and tadalafil. | Class I | Ongoing |
| March 12, 2025 | Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe Recalled by Safecor Health, LLC Recall D-0252-2025 | Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes. | Class II | Ongoing |
| March 12, 2025 | Ergocalciferol Recalled by Safecor Health, LLC Recall D-0250-2025 | Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes. | Class II | Ongoing |
| January 22, 2025 | Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement Recalled by Eclectic Institute Inc Recall F-0401-2025 | Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger Fruit and their quantities were not listed correctly in the Supplement Facts panel. | Class III | Terminated |
| January 1, 2025 | ZOE brand Daily 30+ Prebiotic blend Recalled by Zoe US, Inc. Recall F-0316-2025 | Product may contain foreign objects: small metal pieces and/or stones | Class II | Terminated |
| December 18, 2024 | DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules Recalled by Deseret Biologicals Inc Recall F-0262-2025 | Product contains undeclared soy lecithin. | Class II | Terminated |
| November 27, 2024 | Douglas Labs Stress-B-Plus Dietary Supplement Recalled by Nestle Product Technology Center – Nestle Health Science Recall F-0139-2025 | Nestle Health Science (NHS U.S., LLC) is initiating a recall of Douglas Labs Stress-B-Plus Dietary Supplement Tablets, 90 tablets per bottle. The bottle is white and made of plastic. Lot Numbers 50335944,50344396, expiration date 04/11/2026. The product is… | Class II | Terminated |
Product names and reasons are copied from the FDA records and shortened. “Reported” is the date of the FDA Enforcement Report; the company may have started the recall earlier. Search the recall number in the FDA Enforcement Report for lot codes, dates and where the product was sold.
What Class I, II and III mean
- Class I: the most serious. There is a reasonable chance that using the product will cause serious health problems or death.
- Class II: using the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Class III: using the product is not likely to cause health problems (for example, a labeling error).
Source: the FDA’s recall background and definitions.
Launches we reviewed: FDA recall check
For each supplement launch reviewed on this site, our software searches the FDA’s enforcement records (all dates) for the product’s name.
- Arctic Blast review: no FDA recall found under that name (November 9, 2026).
- Cardio Shield review: no FDA recall found under that name (November 9, 2026).
- Finessa review: no FDA recall found under that name (November 9, 2026).
- Java Burn review: no FDA recall found under that name (November 9, 2026).
- Liv Pure review: no FDA recall found under that name (November 9, 2026).
- Phytomem One review: no FDA recall found under that name (November 9, 2026).
- Pineal Guardian X review: no FDA recall found under that name (November 9, 2026).
- Protoflow review: no FDA recall found under that name (November 9, 2026).
- VenoPlus 8 review: no FDA recall found under that name (November 9, 2026).
“No recall found” only means the FDA has not posted a recall under that product name. It doesn’t mean a product is safe or that it works, and products are sometimes sold under several names. Each review lists who should skip the product and the medication interactions to ask a doctor about.
If you have a recalled product
- Compare the lot code and dates on your package with the FDA record: not every lot is always recalled.
- Stop using it and follow the company’s or the store’s instructions for a refund or return.
- If you think it made you sick, talk to your doctor, and report it to the FDA through MedWatch.
What this page doesn’t tell you
- Not every problem becomes a recall. The FDA also warns about tainted products sold as supplements without a formal recall: see its Health Fraud Product Database.
- The FDA posts recalls in weekly reports, so the newest ones can take a week or more to show up here. The FDA’s recalls page lists company announcements as they come out.
- The list covers records whose product description says “supplement”; a supplement described another way can be missing.
Sources: openFDA enforcement reports (food and drug), checked November 9, 2026; FDA Enforcement Report.
General information, not medical advice. Talk to your doctor before starting a supplement, especially if you are pregnant, nursing, take medication or have a medical condition.