Dietary supplements recalls: brands, lot codes and what to do
Short answer: FDA has listed 82 dietary supplements recalls reported since November 2024; the most recent was reported on Oct 28, 2026 (EVEXIAS HEALTH SOLUTION). Recalls cover specific products, lots and dates. Compare your package with the list below.
Search all FDA food recalls by product, brand, UPC or lot code.
All 82 recalls
Recall details
EVEXIAS HEALTH SOLUTION · Oct 28, 2026
- Product
- Evexias Health Solutions Amino Ultra, 90-capsules, dietary supplement in white plastic bottles with blue/green/white labeling
- Why it was recalled
- The product is mislabeled and fails to declare fish oil.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- " Lot Number: 594886001 MFG 1125, printed on side label. " Affected units only: Bottles with 496 inkjet-printed on the bottom
- How many
- 30 bottles
- Where it was sold
- FL, NM, PA, NY, TN, SD, ND, KY, WA
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 24, 2026; FDA classified it on Oct 21, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0170-2027
PRIMAL SUPPLEMENTS GROUP LLC · Oct 28, 2026
- Product
- PRIMAL HERBS, VOLUME, HERBAL SUPPLEMENT, Net Wt. 8.5 oz, 30 servings
- Why it was recalled
- FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- All orders placed between July 2, 2025, and September 19, 2025, on the website: primalherbs.com
- How many
- Unknown
- Where it was sold
- Product was sold on the website primalherbs.com
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 27, 2026; FDA classified it on Oct 21, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0172-2027
Pacific Health Sciences Llc · Oct 28, 2026
- Product
- Babies' Magic Tea; Baby Sleep Gripe Water; Dietary Supplement; Net Wt. 4 OZ; Age 2eeks+ "No Alcohol, Dairy, Wheat, Soy And Animal Testing" UPC: 850302008183
- Why it was recalled
- Adulterated (elevated levels of alcohol) infant dietary supplement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25122bw Expiration date: 12/2028
- How many
- 953 units
- Where it was sold
- Product was manufactured for a single customer located in Florida. Product was made available through Amazon and through the customers website.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Oct 6, 2026; FDA classified it on Oct 21, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0168-2027
A&P CREATIONS · Oct 14, 2026
- Product
- X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714.
- Why it was recalled
- Product contains undeclared Sildenafil and Tadalafil.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.
- How many
- 1,283 retail units
- Where it was sold
- Distributed nationwide (US).
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 14, 2026; FDA classified it on Oct 7, 2026; reported in FDA's enforcement report on Oct 14, 2026.
- FDA recall number
- H-0016-2027
Byron White Formulas, Inc. · Sep 2, 2026
- Product
- Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
- Why it was recalled
- Label does not declare walnuts in English
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot Code Format = MMD,DYY: 022,224. 061,424. 092,324. 022,125. 071,825. 112,125. 040,826.
- How many
- 10,403 units
- Where it was sold
- Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 11, 2026; FDA classified it on Aug 26, 2026; reported in FDA's enforcement report on Sep 2, 2026.
- FDA recall number
- H-1278-2026
ZMB Enterprises · Sep 2, 2026
- Product
- Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- Why it was recalled
- The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Sold between July - December 2025
- How many
- unknown
- Where it was sold
- The firm markets their products online via their website addallxr.com
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Apr 3, 2026; FDA classified it on Aug 24, 2026; reported in FDA's enforcement report on Sep 2, 2026.
- FDA recall number
- H-1263-2026
Byron White Formulas, Inc. · Sep 2, 2026
- Product
- Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
- Why it was recalled
- Label does not declare walnuts in English
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot Code Format = MMD,DYY: 120,623. 031,824. 070,324. 100,224. 041,425. 101,625.
- How many
- 3,486 units
- Where it was sold
- Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 11, 2026; FDA classified it on Aug 26, 2026; reported in FDA's enforcement report on Sep 2, 2026.
- FDA recall number
- H-1277-2026
Byron White Formulas, Inc. · Sep 2, 2026
- Product
- Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
- Why it was recalled
- Label does not declare walnuts in English
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot Code Format = MMD,DYY: 012,324. 041,924. 062,824. 092,024. 101,624. 111,324. 071,425. 093,025. 012,026. 042,826.
- How many
- 18,791 units
- Where it was sold
- Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 11, 2026; FDA classified it on Aug 26, 2026; reported in FDA's enforcement report on Sep 2, 2026.
- FDA recall number
- H-1276-2026
FACTORY6, INC. · Aug 12, 2026
- Product
- Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administration: OraI. Manufactured for Zen Principle 774 Mays Blvd Incline Village, NV 89451. The product is offered as a 1-pack (180 capsules; Amazon code/FNSKU X000ZJJ4FT) and as a 2-pack (twin pack, 360 capsules; Amazon code/FNSKU X00159YJXP).
- Why it was recalled
- Possible Salmonella in Moringa Leaf Powder product. Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- LOT: A6FF4, Best By: 11/2028
- How many
- 2,048 bottles
- Where it was sold
- Distributed to Nevada for further distribution.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jul 19, 2026; FDA classified it on Aug 5, 2026; reported in FDA's enforcement report on Aug 12, 2026.
- FDA recall number
- H-1222-2026
Mellish Island Corp · Aug 5, 2026
- Product
- Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3
- Why it was recalled
- Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: CA1G24 Expiration: 08-2027
- How many
- 1,600 bottles
- Where it was sold
- Product is distributed through TikTok exclusively. Presumably nationwide.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jul 1, 2026; FDA classified it on Jul 28, 2026; reported in FDA's enforcement report on Aug 5, 2026.
- FDA recall number
- H-1190-2026
Modern Warrior Life, LLC · Jul 29, 2026
- Product
- Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
- Why it was recalled
- FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Product distributed between April of 2022 until December 8th of 2025.
- How many
- Unknown
- Where it was sold
- The recalled product was distributed to customers nationwide from April 2022 until December 8, 2025
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jan 9, 2026; FDA classified it on Jul 17, 2026; reported in FDA's enforcement report on Jul 29, 2026.
- FDA recall number
- H-1178-2026
MOGO Moringa LLC · Jul 8, 2026
- Product
- MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, SUPPLEMENT FACTS MORINGA POWDER 1050 mg, Ingredients: 100% Pure Moringa Leaf Powder (Moringa Oleifera), MANUFACTURED IN USA AND Marketed by: MOGO MIRINGA LLC, PO BOX 32066 Saint Louis, MO 63132
- Why it was recalled
- Product may be contaminated with Salmonella Typhimurium Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028
- How many
- 23,186 bottles
- Where it was sold
- Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 24, 2026; FDA classified it on Jun 29, 2026; reported in FDA's enforcement report on Jul 8, 2026.
- FDA recall number
- H-1128-2026
Provision Health Corp. dba PH Labs · Jul 8, 2026
- Product
- Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023
- Why it was recalled
- Dietary supplement product Vista MAX contains undeclared Yellow#5.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
- How many
- 6,967 units across all lots
- Where it was sold
- Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 18, 2026; FDA classified it on Jul 1, 2026; reported in FDA's enforcement report on Jul 8, 2026.
- FDA recall number
- H-1135-2026
Provision Health Corp. dba PH Labs · Jul 8, 2026
- Product
- Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size: 4 Capsules; Distributed by: L.A. Farmacia Natural, Burbank, CA 91504 UPC: PHF-C023
- Why it was recalled
- Dietary supplement product Ocular Plus contains undeclared Yellow#5.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
- How many
- 6,967 units across all lots
- Where it was sold
- Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 18, 2026; FDA classified it on Jul 1, 2026; reported in FDA's enforcement report on Jul 8, 2026.
- FDA recall number
- H-1134-2026
SENSORY SUPPLEMENT LLC · Jun 17, 2026
- Product
- NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT NUTRITIONAL SUPPLEMENT TO SUPPORT DRAIN AND GUT HEALTH NET WT. 5.9 OZ; UPC: 310M5951601
- Why it was recalled
- Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- LOT number: 310M5951601 Expiration: 0250A6 EXP 03/2028
- How many
- 512 units
- Where it was sold
- Product is available nationwide and sold through the firm's online website direct to consumers.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 6, 2026; FDA classified it on Jun 24, 2026; reported in FDA's enforcement report on Jun 17, 2026.
- FDA recall number
- H-1109-2026
Sato Pharmaceutical Inc. · Jun 10, 2026
- Product
- Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml container. Packed in single serving, 3 units/pack, and 10 units per pack. Single UPC: 49873-916-11 3pack UPC: 49873-916-15 10pack UPC: 49873-916-07
- Why it was recalled
- Product does not meet label claim for Vitamin E.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot: Expiration date: single CXW T Jan-27 3pack CXW T Jan-27 10pack PXW Z Mar-26 10pack XXW W Dec-27
- How many
- 25,130 units across all package sizes
- Where it was sold
- Product was distributed to two domestic consignees who further distribute nationwide.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Mar 12, 2026; FDA classified it on Jun 2, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-0892-2026
Llorens Pharmaceuticals International Division, Inc. · May 27, 2026
- Product
- Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400 bottle, 47 SERVING PER BOTTLE, 24 bottles- 8 FL Oz (237mL) Amber PET modern round bottles per package, Store at room. Mnfg by: Llorens Pharmaceutical Miami, FL
- Why it was recalled
- Foreign object: black particulate matter Pieces of foreign material in food can cause injuries such as cuts to the mouth or choking.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: B2025 Expiration Date:08/27
- How many
- 4,196 units
- Where it was sold
- Distributed to MO, IL, NJ, NY, TX, FL, PR, MA, OK, VA, MN, IA, OH, GA, WI, WA, CA, IN, NC, CO, TN, MA, MO, WV, AZ, DE
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 7, 2026; FDA classified it on May 19, 2026; reported in FDA's enforcement report on May 27, 2026.
- FDA recall number
- H-0809-2026
Pure Vitamins and Natural Supplements, LLC · Apr 15, 2026
- Product
- Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Blue Bull Corporation Made In USA. UPC Code 707443349917
- Why it was recalled
- FDA analysis revealed the presence of undeclared sildenafil
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- EXP Date 02/2029
- How many
- Unknown
- Where it was sold
- New Jersey
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Mar 13, 2026; FDA classified it on Apr 7, 2026; reported in FDA's enforcement report on Apr 15, 2026.
- FDA recall number
- H-0654-2026
Pure Vitamins and Natural Supplements, LLC · Apr 15, 2026
- Product
- Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Red Bull Corporation. Turkey www.redbullhoney.com UPC Code 9554100205595
- Why it was recalled
- FDA analysis revealed the presence of undeclared sildenafil
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- B/N ORB524 MFG Date: MAY 2024 EXP DATE: MAY 2029
- How many
- Unknown
- Where it was sold
- New Jersey
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Mar 13, 2026; FDA classified it on Apr 7, 2026; reported in FDA's enforcement report on Apr 15, 2026.
- FDA recall number
- H-0655-2026
Siluetaya, LLC · Apr 1, 2026
- Product
- SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027
- Why it was recalled
- Product contains yellow oleander
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot: US1220, Expiration Date: 06/2027
- How many
- 40 units
- Where it was sold
- Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Oct 29, 2025; FDA classified it on Apr 2, 2026; reported in FDA's enforcement report on Apr 1, 2026.
- FDA recall number
- H-0647-2026
Shaman Botanicals, LLC · Mar 25, 2026
- Product
- Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: White child-resistant plastic bottle with sticker label applied UPC 810057763779 (sometimes proceeded by 00)
- Why it was recalled
- A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- B#AAW.501.3; all expiration dates
- How many
- 97,063 units
- Where it was sold
- Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 13, 2026; FDA classified it on Jun 24, 2026; reported in FDA's enforcement report on Mar 25, 2026.
- FDA recall number
- H-1108-2026
Shaman Botanicals, LLC · Mar 25, 2026
- Product
- Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed silver metallic bag with a front and back sticker for the labels; Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 150mg total 7-Hydroxymitragynine per container (10 Packets x 2 Tablets Each) 7.5mg 7-OH per tablet/serving, LEMON DIETARY SUPPLEMENT Net Wt. 0.17 oz 10 PACKETS 2 TABLETS EACH Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed black flexible plastic bag with multi color sticker label on front and back UPC 810057763724
- Why it was recalled
- A sample of the product had the active ingredient in a quantity greater than the labeled specification.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- B#AAW.501.3; all expiration dates
- How many
- 2 pack: 1281 units; 20-count: 14,491 units
- Where it was sold
- Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 13, 2026; FDA classified it on Jun 24, 2026; reported in FDA's enforcement report on Mar 25, 2026.
- FDA recall number
- H-1107-2026
Ambrosia Brands LLC · Mar 18, 2026
- Product
- Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625 Randall Ave, St. 100, Cheyenne, WY 82001; SUGGESTED USE: As a dietary supplement, take two (2) veggie capsules once a day. For best results, take 20-30 min before a meal with an 8oz. glass of water or as directed by your health professional; UPC: 8 60012 16172 0
- Why it was recalled
- Product may be contaminated with Salmonella Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot # - Expiration Date: 5020591 - 03/2027 5020592 - 03/2027 5020593 - 03/2027 5020594 - 03/2027 5020595 - 03/2027 5020596 - 03/2027 5030246 - 04/2027 5030247 - 04/2027 5030248 - 04/2027 5030249 - 04/2027 5030250 - 04/2027 5030251 - 04/2027 5040270 - 05/2027 5040271 - 05/2027 5040272 - 05/2027 5040273 - 05/2027 5040274 - 05/2027 5040275 - 05/2027 5040276 - 05/2027 5040277 - 05/2027 5040278 - 05/2027 5040279 - 05/2027 5050053 - 6/2027 5050054 - 6/2027 5050055 - 6/2027 5050056 - 6/2027 5060069 - 07/2027 5060070 - 07/2027 5060071 - 07/2027 5060072 - 07/2027 5060073 - 07/2027 5060074 - 07/2027 5060075 - 07/2027 5060076 - 07/2027 5060077 - 07/2027 5060078 - 07/2027 5060079 - 07/2027 5060080 - 07/2027 5080084 - 9/2027 5080085 - 9/2027 5080086 - 9/2027 5090107 - 10/2027 5090108 - 10/2027 5090109 - 10/2027 5090113 - 10/2027 5090114 - 10/2027 5090115 - 10/2027 5090116 - 10/2027 5090117 - 10/2027 5090118 - 10/2027 5100039 - 11/2027 5100048 - 11/2027
- How many
- 1,224,208 units
- Where it was sold
- Nationwide in the United States, including American Samoa, Northern Mariana Islands, Puerto Rico, and Virgin Islands. International distribution to consumers in: Algeria, Anguilla, Australia, Austria, Bahrain, Belgium, Bosnia and Herzegovina, Brazil, Brunei, Bulgaria, Canada, Chile, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Djibouti, Dominican Republic, Egypt, Estonia, Faroe Islands, Finland, France, French Polynesia, Georgia, Germany, Gibraltar, Greece, Hong Kong, Hungary, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Latvia, Lithuania, Luxembourg, Malaysia, Malta, Marshall Islands, Mexico, Nauru, New Zealand, Netherlands, Norway, Oman, Pakistan, Peru, Philippines, Poland, Portugal, Qatar, Romania, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Suriname, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Turkey, United Arab Emirates, United Kingdom, Venezuela, and Zimbabwe.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Feb 13, 2026; FDA classified it on Mar 9, 2026; reported in FDA's enforcement report on Mar 18, 2026.
- FDA recall number
- H-0546-2026
Pure Solutions, Inc. · Feb 25, 2026
- Product
- Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not sold in case lots)
- Why it was recalled
- Label declares bovine colostrum but does not declare milk allergen.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- LOT: 0528D911 Expiration Date: May 2028
- How many
- 442 units (bottles)
- Where it was sold
- Product was distributed to: AR, FL, CO, CA, CT, HI, IN, IL, ID, IA, KS, KY, LA, OH, OK, OR, MA, MI, MN, MO, GA, NC, NE, ND, NY, PA, SC, TN, NJ, UT, TX, VA , WA, WV, WI, WY
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 3, 2026; FDA classified it on Feb 27, 2026; reported in FDA's enforcement report on Feb 25, 2026.
- FDA recall number
- H-0537-2026
TKS Co-pack Manufacturing, LLC · Feb 18, 2026
- Product
- Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Shipping unit: two 15 count decorated boxes in a corrugated Aonic Master Shipper. Firm Name and Address on Label: Aonic Inc. 2261 MarketStreet #5416 San Francisco, CA 94114 USA.
- Why it was recalled
- Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. Some E. coli strains, such as O157:H7, can cause bloody diarrhea and abdominal cramps, and some people develop a type of kidney failure called hemolytic uremic syndrome (HUS).
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot 5349A BB 12/27; Lot 5363A BB 12/27
- How many
- 3630 individual bottles
- Where it was sold
- Distributed to customer in Utah.
- Status
- Completed: the company has finished its recall actions.
- Dates
- Recall started Jan 15, 2026; FDA classified it on Feb 20, 2026; reported in FDA's enforcement report on Feb 18, 2026.
- FDA recall number
- H-0520-2026
TKS Co-pack Manufacturing, LLC · Feb 18, 2026
- Product
- Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Sipping unit: two 15 count decorated boxes in a corrugated Aonic Master Shipper. Firm Name and Address on Label: Aonic Inc. 2261 MarketStreet #5416 San Francisco, CA 94114 USA.
- Why it was recalled
- Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. Some E. coli strains, such as O157:H7, can cause bloody diarrhea and abdominal cramps, and some people develop a type of kidney failure called hemolytic uremic syndrome (HUS).
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot 5349A BB 12/27; Lot 5363A BB 12/27
- How many
- 780 individual bottles
- Where it was sold
- Distributed to customer in Utah.
- Status
- Completed: the company has finished its recall actions.
- Dates
- Recall started Jan 15, 2026; FDA classified it on Feb 20, 2026; reported in FDA's enforcement report on Feb 18, 2026.
- FDA recall number
- H-0521-2026
Imu-Tek Animal Health, Incorporated · Feb 11, 2026
- Product
- Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use this for their pets).Packaging: Plastic jar with Sealed lid. Net Weight: 7 ounces. UPC:7 38654 00033 5 Firm name on label: Imu-Tek, 3541 East Vine Drive, Fort Collins, CO 80524
- Why it was recalled
- Undeclared milk allergen People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot #216, Expiration 4/16/2027
- How many
- 113 bottles
- Where it was sold
- Distributed in : AZ, CA, CO, FL, MA, ME, MN, NC, NH, OK, RI, TN, TX, UT, and WI.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 25, 2025; FDA classified it on Feb 5, 2026; reported in FDA's enforcement report on Feb 11, 2026.
- FDA recall number
- H-0483-2026
SUPERFOODS, INC. · Feb 4, 2026
- Product
- Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 8.5OZ (240G); Manufactured for Superfoods, Inc.; UPC: 860013190804 b.) Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.28oz (8g) STICKS - NET WT. 8.47oz (240g); Manufactured for Superfoods, Inc.; UPC: 850077468063
- Why it was recalled
- Products may be contaminated with Salmonella Typhimurium Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- The lot code is printed on the bottom back of the packaging in black and begins with the letter "A". Expiration dates from 08/2026 to 01/2028. 2024 Lots: AA24H013, A24I019, A24J012, A24J041, A24K019, A24L001, A24L013, A24L036, A24L035 2025 Lots: A25A009, A25A017, A25A018, A25B005, A25B004, A25C018, A25C022, A25D021, A25E005, A25E007, A25F019, A25G033, A25F029, A25G065, A25H005, A25H012, A25I005, A25I010, A25I032, A25J005, A25J028, A25J037, A25K007, A25K013, A25L006 Stick Pack Products: 32825-1, 34425-1
- How many
- 795,834 units (total)
- Where it was sold
- Nationwide, including Puerto Rico, Guam, and Virgin Islands; United Kingdom
- Status
- Completed: the company has finished its recall actions.
- Dates
- Recall started Jan 15, 2026; FDA classified it on Jan 29, 2026; reported in FDA's enforcement report on Feb 4, 2026.
- FDA recall number
- H-0433-2026
SUPERFOODS, INC. · Feb 4, 2026
- Product
- a.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 9.49oz (269.16g); Manufactured for Superfoods, Inc.; UPC: 860013190811 b.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.32oz (9g) STICKS - NET WT. 9.52oz (270g); Manufactured for Superfoods, Inc.; UPC: 850077468070
- Why it was recalled
- Products may be contaminated with Salmonella Typhimurium Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- The lot code is printed on the bottom back of the packaging in black and begins with the letter "A". Expiration dates from 08/2026 to 01/2028. 2024 Lots: A24G012, A24I036, A24J005, A24J032, A24J037, A24K028, A24L014, A24L019, A24L032 2025 Lots: A25A005, A25A058, A25B006, A25D010, A25D036, A25D041, A25E008, A25F021, A25H009, A25H030, A25H045, A25I011, A25J036, A25K035 Stick Pack Products: 32925-1, 34525-1
- How many
- 795,834 units (total)
- Where it was sold
- Nationwide, including Puerto Rico, Guam, and Virgin Islands; United Kingdom
- Status
- Completed: the company has finished its recall actions.
- Dates
- Recall started Jan 15, 2026; FDA classified it on Jan 29, 2026; reported in FDA's enforcement report on Feb 4, 2026.
- FDA recall number
- H-0434-2026
GOLD STAR DISTRIBUTION INC · Jan 28, 2026
- Product
- All human food products distributed from the firm. Including but not limited to: snack foods, candy, gum, cooking oil, canned fruit and beans, honey, Dietary supplements, peanut butter, oatmeal, rice, dry peas and beans, ramen, cold cereal, hot sauce, lemon juice, crackers, canned sardines tuna and Oyster, sauces, seasonings, sugar, bottled and canned beverages, coffee and filters and creamer, tea bags, canned pasta, dates, flour, baby food
- Why it was recalled
- Potential exposure of rodents and rodent activity in the distribution center.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- all codes of products purchased from this firm.
- How many
- unknown
- Where it was sold
- IN, MN, ND
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Dec 26, 2025; FDA classified it on Jan 22, 2026; reported in FDA's enforcement report on Jan 28, 2026.
- FDA recall number
- H-0411-2026
Herbs Forever · Jan 21, 2026
- Product
- HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3
- Why it was recalled
- Potential undeclared allergen ingredient (Wheat) People who are allergic to wheat, or who have celiac disease, run the risk of a serious reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Batch: 124-4 Expiration date: 1/2029
- How many
- 45 units
- Where it was sold
- Product is sold primarily on-line nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 6, 2026; FDA classified it on Jan 14, 2026; reported in FDA's enforcement report on Jan 21, 2026.
- FDA recall number
- H-0404-2026
Herbs Forever · Jan 21, 2026
- Product
- HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
- Why it was recalled
- Potential undeclared allergen ingredient (Wheat) People who are allergic to wheat, or who have celiac disease, run the risk of a serious reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Batch: 622-2 Expiration date: 6/2029
- How many
- 45 units
- Where it was sold
- Product is sold primarily on-line nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 6, 2026; FDA classified it on Jan 14, 2026; reported in FDA's enforcement report on Jan 21, 2026.
- FDA recall number
- H-0405-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- C132GR EXP 7/27 C131GR EXP 6/27 C121GR EXP 2/27 C115GR EXP 12/26 C108GR EXP 1/26 C93GR EXP 7/25
- How many
- 48 bags
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0346-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- T720CH EXP 3/30 T656CH EXP 10/29 T618CH EXP 7/29 T568CH EXP 1/29 T532CH EXP 10/28
- How many
- 144 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0344-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thyme, Oregon Grape Root, & Bentonite Clay, 50 capsules/510 mg; packaged in a plastic bag
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25
- How many
- 38 bags
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0348-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass dropper bottle, UPC 283162814429
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28
- How many
- 116 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0340-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- T553MF EXP 12/28
- How many
- 22 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0345-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25
- How many
- 275 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0347-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- T848B EXP 11/30 T836B EXP 10/30 T808B EXP 9/30 T771B EXP 7/30 T723B EXP 3/30 T696B EXP 1/29 T655B EXP 10/29 T594B EXP 4/29 T536B EXP 10/28
- How many
- 278 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0343-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip, Chamomile, Vegetable Glycerin, water; packaged in a 2 oz. glass dropper bottle
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- E164BS EXP 1/27 E128BS EXP 7/26
- How many
- 49 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0342-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 249953949282
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- E166SA EXP 4/28
- How many
- 23 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0341-2026
Avion Pharmaceuticals, LLC · Dec 10, 2025
- Product
- Prenate Chewable¿ A chewable Rx prenatal vitamin with a delicious chocolate flavor with Quatrefolic Dietary Supplement 30 Tablets Rx Only UPC 3 75854 30630 2 Manufactured for: Avion Pharmaceuticals, LLC Alpharetta, GA 30005
- Why it was recalled
- 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. People who are allergic to soy run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Product Code 75854-306-30 Lot 2402036 Exp 2026-04 Lot 2402036A Exp 2026-04 & Lot 2412020 Exp 2027-02
- How many
- 804 bottles
- Where it was sold
- Product was shipped to the following states: AL, AZ, CA, CO, FL, GA, IA, IL, KY, MA, MO, NY, OH, OK, PA, TX & VA.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Oct 29, 2025; FDA classified it on Dec 3, 2025; reported in FDA's enforcement report on Dec 10, 2025.
- FDA recall number
- H-0233-2026
Water Pure, Inc. · Dec 10, 2025
- Product
- My Bladder; Supports normal bladder tone & control; Dietary Supplement; packaged in white HDPE bottle with a white cap; bottle size is 150 CC; the net contents in 60 clear capsules containing brown powder
- Why it was recalled
- Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303 Some E. coli strains, such as O157:H7, can cause bloody diarrhea and abdominal cramps, and some people develop a type of kidney failure called hemolytic uremic syndrome (HUS).
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot Number: 03042517
- How many
- 17,612 bottles
- Where it was sold
- Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 24, 2025; FDA classified it on Nov 28, 2025; reported in FDA's enforcement report on Dec 10, 2025.
- FDA recall number
- H-0213-2026
MeriCal, LLC · Dec 3, 2025
- Product
- Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775
- Why it was recalled
- Potential contamination of Salmonella Richmond Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- 500-00055034; 500-00055035; 500-00055036; 500-00055037; 500-00055038; 500-00055039 500-00055040; 500-00055042; 500-00055043; 500-00055044; 500-00055045; 500-00055046 500-00055047; 500-00055048; 500-00055049; 500-00055050; 500-00055051; 500-00055052 500-00055053; 500-00055054; 500-00055055; 500-00055056; 500-00055057; 500-00055058 500-00056121; 500-00056122; 500-00056123; 500-00056124; 500-00056125; 500-00056126 500-00056127; 500-00056128; 500-00056129; 500-00056130; 500-00056131; 500-00056132 500-00056133; 500-00056134; 500-00056135; 500-00056136; 500-00056137; 500-00056138 500-00056139; 500-00056140; 500-00056141; 500-00056142; 500-00056143; 500-00056144 500-00056145; 500-00056146; 500-00056147; 500-00056148; 500-00056149; 500-00056150 500-00056151; 500-00056152; 500-00056153; 500-00056154; 500-00056155; 500-00056230 500-00056231; 500-00056318; 500-00056323; 500-00056429; 500-00056772;
- How many
- 698,064 units
- Where it was sold
- Product was distributed to consignee locations across the country.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Oct 24, 2025; FDA classified it on Nov 21, 2025; reported in FDA's enforcement report on Dec 3, 2025.
- FDA recall number
- H-0205-2026
Organicare Nature's Science, LLC · Oct 15, 2025
- Product
- FemiClear Daily Bladder Strength Dietary Supplement, 28 Count, UPC 817008020684, SKU FEM50060
- Why it was recalled
- Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303. Some E. coli strains, such as O157:H7, can cause bloody diarrhea and abdominal cramps, and some people develop a type of kidney failure called hemolytic uremic syndrome (HUS).
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot 111924176
- How many
- 15,075 bottles (28 ct per bottle)
- Where it was sold
- Retail stores in all 50 states and Puerto Rico and via e-commerce
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 4, 2025; FDA classified it on Oct 9, 2025; reported in FDA's enforcement report on Oct 15, 2025.
- FDA recall number
- H-0031-2026
M.O.M Enterprises, LLC. · Oct 15, 2025
- Product
- Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with elderberry & vitamin C; LIQUID DIETARY SUPPLEMENT; AGE 4 MONTHS+, NET WT. 2 OZ (60 ML)
- Why it was recalled
- Potential yeast contamination.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot code: 25100, 25148, 25155 UPC: 679234051814 EXP 04/2027, 05/2027, 06/2027
- How many
- 46,752 units/bottles (Lot 25100: 8,424 units; Lot 25148: 16,488 units; Lot 25155: 21,840 units)
- Where it was sold
- AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 12, 2025; FDA classified it on Oct 7, 2025; reported in FDA's enforcement report on Oct 15, 2025.
- FDA recall number
- H-0025-2026
Vitalabs, Inc. · Oct 8, 2025
- Product
- vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black Girl Vitamins 60 gummies UPC 8 60008 57505 0 Manufactured for: Black Girl Vitamins 601 W Harrison St., Chicago, IL 60607. 2. Rise-N-Shine 17 Woodport Road, Sparta, NJ 07871 UPC 8 99130 01189 1
- Why it was recalled
- Undeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts. People who are allergic to peanuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- 1. LOT# 57221A BEST BY: 07/2026 and Lot# 56199 Best By: 07/2026 2. Lot# 57664 Best By: 07/2026
- How many
- 9,657 bottles
- Where it was sold
- Product was shipped to IL & NJ.
- Status
- Completed: the company has finished its recall actions.
- Dates
- Recall started Jun 13, 2025; FDA classified it on Oct 10, 2025; reported in FDA's enforcement report on Oct 8, 2025.
- FDA recall number
- H-0037-2026
Extract Labs, Inc. · Oct 1, 2025
- Product
- Blue Razz 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Blue Razz: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)
- Why it was recalled
- Potential peanut protein cross-contact.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25JD082307A EXP: 07/2027 Printed on bulk bag identifier adhesive
- How many
- 19,810 gummies
- Where it was sold
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 26, 2025; FDA classified it on Sep 22, 2025; reported in FDA's enforcement report on Oct 1, 2025.
- FDA recall number
- H-0623-2025
Extract Labs, Inc. · Oct 1, 2025
- Product
- Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg CBD and 10mg D9 THC per gummy Dosage: 1 gummy Form: Gummy Administration: Oral Intended use: Dietary Supplement Type of packaging: 225cc amber packer bottle with child-resistant cap and inner pressure seal Net wt: 3.53oz UPC: 850029647928 Firm name & address: Extract Labs, Inc., 1399 Horizon Ave, Lafayette, CO 80026
- Why it was recalled
- Potential peanut protein cross-contact.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25E5082907A (we call this a batch ID) EXP: 07/2027 Printed on the bottom of the bottle
- How many
- 2180 gummies (109/20 ct bottles)
- Where it was sold
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 26, 2025; FDA classified it on Sep 22, 2025; reported in FDA's enforcement report on Oct 1, 2025.
- FDA recall number
- H-0621-2025
Extract Labs, Inc. · Oct 1, 2025
- Product
- Elderberry 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Elderberry: 24 bags x 5kg and 1 bag x 3.6kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)
- Why it was recalled
- Potential peanut protein cross-contact.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25JD072107A EXP: 07/2027 Printed on bulk bag identifier adhesive
- How many
- 19,720 gummies
- Where it was sold
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 26, 2025; FDA classified it on Sep 22, 2025; reported in FDA's enforcement report on Oct 1, 2025.
- FDA recall number
- H-0622-2025
Extract Labs, Inc. · Oct 1, 2025
- Product
- Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Mai Tai: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)
- Why it was recalled
- Potential peanut protein cross-contact.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25JD042507A EXP: 07/2027 Printed on bulk bag identifier adhesive
- How many
- 19,750 gummies
- Where it was sold
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 26, 2025; FDA classified it on Sep 22, 2025; reported in FDA's enforcement report on Oct 1, 2025.
- FDA recall number
- H-0624-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 SERVINGS SUPPORTS ENERGY PRODUCTION PROTEN ANTIOXIDANT PROPERTIES SUPPORTS HEALTHY BLOOD SUGAR LEVELS NET WT. 8.12OZ (250g) DIETARY SUPPLEMENT UPC 6 89466 70601 7 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims and Misbranded.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 710581618 Exp Date 12/26
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0598-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- Top Secret Nutrition extra strength uric control fast acting multi-pronged uric acid control 30 veggie caps DIETARY SUPPLEMENT UPC 8 11226 02158 4 Distributed by: TOP SECRET NUTRITION, LLC 6015-B Unity Dr. Norcross, GA 30052
- Why it was recalled
- Unapproved Drug Claims.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot C1238 Exp Date 01/25
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0599-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- HI-TECH PHARMACEUTICALS PINE BARK SUPPORTS HEART HEALTH & CIRCULATION SUPPORTS CARDIOVASCULAR HEALTH FIGHTS OXIDATIVE STRESS 60 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02446 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims and Misbranded.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot C15Cl4 Exp Date 10/26
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0592-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS RESPIRATORY HEALTH SUPPORTS CARDIOVASCULAR HEALTH 120 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02491 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims and Misbranded.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot C1612 Exp Date 08/27
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0594-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH PHARMECEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 059960809 Exp Date 06/28
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0591-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT PEACH MANGO NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 38302 40906 3 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims and Misbranded.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 202140114 Exp Date 03/27
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0600-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- IFN iFORCE NUTRITION JOINT HELP HEALTHY JOINTS & LIGAMENTS DIETARY SUPPLEMENT 120 CAPSULES UPC 8 54503 00226 5 Manufactured By: iForce Nutrition 6015B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 101330812 Exp Date 01/25
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0595-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT WATERMELON NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 38302 40905 6 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims and Misbranded.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 174271126 Exp Date 09/26
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0601-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT KIWI-STRAWBERRY NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 89466 70619 2 Manufactured by: Prime Nutrition 6015-b Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims and Misbranded.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 207460659 Exp Date 10/25
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0597-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH PCT LEGAL GEAR DIETARY SUPPLEMENT 17-PROANDRO pBOLD FORM-XT UPC 7 44890 94151 6 MADE FOR LG SCIENCES 6015-B UNITY DR. NORCROXX, GA 30071
- Why it was recalled
- Unapproved Drug Claims.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot Cl 78216691877 Exp Date 02/28
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0596-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolutionary Joint Support System 90CT UPC 8 57084 00035 4 Hi-Tech Pharmaceuticals, Inc. 6015-B Unity Dr Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 503110607 Exp Date 04/30
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0590-2025
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP-1) RECEPTOR AGONIST AND SECRETAGOGUES NOVEL GIP (GLUCOSE-DEPENDENT ISNULINOTROPIC POLYPEPTIDE) RECEPTOR AGONIST 180 TABLETS DIETARY SUPPLEMENT
- Why it was recalled
- Unapproved Drug Claims and Misbranded.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot C19El8 Exp Date 05/30
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0593-2025
M.O.M Enterprises, LLC. · Sep 17, 2025
- Product
- Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with elderberry & vitamin C; LIQUID DIETARY SUPPLEMENT; AGE 4 MONTHS+, NET WT. 2 OZ (60 ML)
- Why it was recalled
- Potential for spoilage due to yeast contamination.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot code: 25084; 25086; UPC: 679234051814 EXP 03/2027
- How many
- 85,248 units/bottles (Lot 25084: 51,096 units; Lot 25086: 34,152 units)
- Where it was sold
- AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, VA, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 5, 2025; FDA classified it on Sep 8, 2025; reported in FDA's enforcement report on Sep 17, 2025.
- FDA recall number
- H-0576-2025
Dynamic Sports Nutrition · Sep 17, 2025
- Product
- Anabolic Research WINN-50 (vanazolol). Dietary Supplement. 90 Capsules. UPC 8 51840-00707 6. Manafactured For: Anabolic Research, 6942 FM 1960 E. #346, Humble, TX 77346-2706.
- Why it was recalled
- Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- LOT: 2307149 MFG: 07/2023
- How many
- 1,566 bottles -2.4 oz each
- Where it was sold
- Nationwide
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jul 28, 2025; FDA classified it on Sep 5, 2025; reported in FDA's enforcement report on Sep 17, 2025.
- FDA recall number
- H-0573-2025
GMP Laboratories of America Inc · Aug 20, 2025
- Product
- Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed by Enjoy Nutirtion, LLC. San Francisco, CA 94108, (415) 894-0537 2.5 mg UPC#: X001SBI13J 5 mg UPC#: X000PY16Z5 10 mg UPC#: X000T9B9B7 20 mg UPC#: X001VBLW8H 1000 MCG UPC#: X003SBV661
- Why it was recalled
- Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- 2.5mg Lot #: 21166, 21640, 21821, 22281, 22757 Expire date: 11/2025, 09/2026, 05/2027, 02/2028 5 mg Lot#: 21123, 21300, 21498, 21783, 21994, 22218, 22299, 22457, 22718 Expire date: 10/2025, 05/2026, 08/2026, 01/2027, 04/2027, 05/2027, 08/2027, 02/2028 10mg Lot#: 21107, 21181, 21288, 21371, 21499, 21695, 21993, 22105, 22200, 22399, 22556, 22650, 22736 Expire date: 10/2025, 12/2025, 02/2026, 03/2026, 05/2026, 07/2026, 01/2027, 01/2027, 03/2027, 07/2027, 10/2027, 01/2028, 02/2029 20mg Lot#: 21301, 21505, 21911, 22106, 22257, 22397, 22557, 22918 Expire date: 02/2026, 05/2026, 10/2026, 05/2027, 07/2028, 10/2027, 04/2028 1000 MCG Lot#: 21442, 22647 Expire date: 05/2025, 01/2027
- How many
- ~185,482 capsules
- Where it was sold
- Distribution was to a single customer who received product in California and Oklahoma.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 24, 2025; FDA classified it on Aug 8, 2025; reported in FDA's enforcement report on Aug 20, 2025.
- FDA recall number
- H-0448-2025
GMP Laboratories of America Inc · Aug 20, 2025
- Product
- Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 Sutter St., Suite 405, San Fransisco, CA 94108 2.5 mg UPC#: X002T4OPLL 10 mg UPC#: X0031AXVE9
- Why it was recalled
- Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- 2.5mg Lot #: 21822 Expire date: 09/2026 10mg Lot#: 21108; 22649 Expire date: 10/2025; 01/2028
- How many
- ~185,482 capsules
- Where it was sold
- Distribution was to a single customer who received product in California and Oklahoma.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 24, 2025; FDA classified it on Aug 8, 2025; reported in FDA's enforcement report on Aug 20, 2025.
- FDA recall number
- H-0447-2025
Preventics, Inc. dba Legere Pharmaceuticals · Jul 2, 2025
- Product
- Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
- Why it was recalled
- Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Batch codes: 21635-21, 21635-22, 21635-23, 21635-34
- How many
- 42,280 capsules
- Where it was sold
- Distributed Nationwide in the United States.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 30, 2025; FDA classified it on Jun 25, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0096-2025
Preventics, Inc. dba Legere Pharmaceuticals · Jul 2, 2025
- Product
- Prothin, dietary supplement. Seven Packets containing 2 tablets and 4 capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
- Why it was recalled
- Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- 12131
- How many
- 1696 bags
- Where it was sold
- Distributed Nationwide in the United States.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 30, 2025; FDA classified it on Jun 25, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0091-2025
Preventics, Inc. dba Legere Pharmaceuticals · Jul 2, 2025
- Product
- Probese Caps, dietary supplement with Iron. 90-count bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
- Why it was recalled
- Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- 21874-19; 21874-20; 21874-21; 21874-22; 21874-23; 21874-24; 21874-25
- How many
- 112,506 pills
- Where it was sold
- Distributed Nationwide in the United States.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 30, 2025; FDA classified it on Jun 25, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0094-2025
Preventics, Inc. dba Legere Pharmaceuticals · Jul 2, 2025
- Product
- Super ProTHIN Plus, dietary supplement. Seven Packets with 2 tablets & 4 Capsules and 1 packet with 14 Nutrilean capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
- Why it was recalled
- Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- 12131
- How many
- 55,080 pills
- Where it was sold
- Distributed Nationwide in the United States.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 30, 2025; FDA classified it on Jun 25, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0092-2025
Preventics, Inc. dba Legere Pharmaceuticals · Jul 2, 2025
- Product
- NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
- Why it was recalled
- Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- 21745-11, 21745-12, 21745-13, 21745-14, 21745-15
- How many
- 94,190 capsules
- Where it was sold
- Distributed Nationwide in the United States.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 30, 2025; FDA classified it on Jun 25, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0095-2025
Preventics, Inc. dba Legere Pharmaceuticals · Jul 2, 2025
- Product
- Protrim Plus, dietary supplement. 90 capsule/bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
- Why it was recalled
- Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- 21634-9
- How many
- 763 Containers
- Where it was sold
- Distributed Nationwide in the United States.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 30, 2025; FDA classified it on Jun 25, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0093-2025
Nordic Naturals, Inc. · Jun 11, 2025
- Product
- Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case
- Why it was recalled
- Product is mislabeled.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot: 244423 RUS-30127 Expiration 05/2026
- How many
- 1164 bottles (120 gummies/bottle)
- Where it was sold
- Domestic: AK, AZ, CA, CO, FL, GA, ID, IN, MA, MT, NC, ND, NH, NV, NY, OK, OR, RI, UT, WA; Foreign: Great Britain, UAE
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 2, 2025; FDA classified it on Jun 3, 2025; reported in FDA's enforcement report on Jun 11, 2025.
- FDA recall number
- F-0840-2025
Supplement Manufacturing Partner Inc. · Apr 30, 2025
- Product
- Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottle/lid, 120 count.Supplement Facts: Spermidine 3HCL 10mg*** Other Ingredients: Hydroxypropyl Methylcellulose, Rice Flour
- Why it was recalled
- Undeclared allergen: Wheat People who are allergic to wheat, or who have celiac disease, run the risk of a serious reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot 12792402-44
- How many
- 6,465 bottles
- Where it was sold
- Product was distributed throughout the United States and Germany.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 4, 2025; FDA classified it on Apr 22, 2025; reported in FDA's enforcement report on Apr 30, 2025.
- FDA recall number
- F-0729-2025
MTN OPS, LLC · Apr 16, 2025
- Product
- MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement, 60 Capsule Bottle (30 Serving). Manufactured exclusively for MTN OPS, LLC, 251 S Mountain Rd., Fruit Heights, UT. UPC 8 40359 40458 2
- Why it was recalled
- Undeclared soy flour People who are allergic to soy run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Expiration Date: 03/2026, Lot# 012324177
- How many
- 7546 bottles
- Where it was sold
- Distributed nationwide except RI and distributed in Canada
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 25, 2025; FDA classified it on Apr 9, 2025; reported in FDA's enforcement report on Apr 16, 2025.
- FDA recall number
- F-0698-2025
Bioriginal Food & Science Corporation · Apr 9, 2025
- Product
- Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml, Dietary Supplement, Black HDPE plastic bottle with cap, Manufactured for Natural Slim, San Juan Puerto Rico
- Why it was recalled
- Undeclared allergens: Soy lecithin People who are allergic to soy run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot Code: PRP403337
- How many
- 61 bottles
- Where it was sold
- Puerto Rico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 21, 2025; FDA classified it on Apr 14, 2025; reported in FDA's enforcement report on Apr 9, 2025.
- FDA recall number
- F-0709-2025
Veridance Pharmacal, LLC · Apr 2, 2025
- Product
- Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use: 1-3 capsules per day with meals, Distributed by: McDonagh Medical Center Gladstone, MO 64119
- Why it was recalled
- Levels of iodine exceeding label claim
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- UPC: 850038221294, Lot codes: 0311-01 exp. 3/26, 0311-02 exp. 3/26, 0367-01 exp. 8/26
- How many
- 450 bottles
- Where it was sold
- One customer located in Gladstone, MO
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 10, 2025; FDA classified it on Mar 27, 2025; reported in FDA's enforcement report on Apr 2, 2025.
- FDA recall number
- F-0671-2025
Eclectic Institute Inc · Jan 22, 2025
- Product
- Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363 52002 2. Eclectic Institute, Inc. 755 NE 6th Street Gresham, OR 97030. The affected label declared "Oregon Grape 190mg ***Oregon Grape 97mg***Cayenne Root (Allium sativum) 195mg ***Ginger Fruit (Capsicum annuum) 65mg***".
- Why it was recalled
- 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.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 25183; Exp date 10/2024 Lot 25543; Exp Date 03/2025
- How many
- 1334 bottles
- Where it was sold
- nationwide
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 3, 2022; FDA classified it on Jan 15, 2025; reported in FDA's enforcement report on Jan 22, 2025.
- FDA recall number
- F-0401-2025
Zoe US, Inc. · Jan 1, 2025
- Product
- ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
- Why it was recalled
- Product may contain foreign objects: small metal pieces and/or stones Pieces of foreign material in food can cause injuries such as cuts to the mouth or choking.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288
- How many
- 142 units
- Where it was sold
- Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Illinois, Kentucky, Maine, Massachusetts, Michigan, Minnesota, New Jersey, New Mexico, New York, North Carolina, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Dec 4, 2024; FDA classified it on Dec 24, 2024; reported in FDA's enforcement report on Jan 1, 2025.
- FDA recall number
- F-0316-2025
Deseret Biologicals Inc · Dec 18, 2024
- Product
- DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, 30 count in a Blue PET bottle with a White cap. Supplement facts declare Phosphatidylserine (from non-GMO sunflower lecithin powder) 40 mg. Distributed by Deseret Biologicals Inc 469 West Parkland Dr, Sandy, UT.
- Why it was recalled
- Product contains undeclared soy lecithin. People who are allergic to soy run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- LOT 020323126 MFG 04/2023
- How many
- 2547 bottles
- Where it was sold
- Distributed nationwide, one foreign distributor to Australia. No DOD distribution. No VA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 30, 2024; FDA classified it on Dec 9, 2024; reported in FDA's enforcement report on Dec 18, 2024.
- FDA recall number
- F-0262-2025
Nestle Product Technology Center - Nestle Health Science · Nov 27, 2024
- Product
- Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944 and 50344396. Expiration Date 04/11/2026
- Why it was recalled
- 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 being recalled because of Incorrect formulation manufactured vs label claims. Product was manufactured with Niacin (as Nicotinic acid) and supplement facts panel states contains Niacin (as Niacinamide). Pieces of foreign material in food can cause injuries such as cuts to the mouth or choking.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot Codes: 50335944, 50344396
- How many
- 3,269 bottles in market
- Where it was sold
- AK,AZ,CA,CO,DE,FL,GA,IA,ID,IL,IN,KS,KY,LA,MA,MD,MI,MN,MO,NC,NH,NJ,NM,NY,OH,OK,OR,PA,SD,TN,TX,VA,WA,WI,WV
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 7, 2024; FDA classified it on Nov 17, 2024; reported in FDA's enforcement report on Nov 27, 2024.
- FDA recall number
- F-0139-2025
What to do
- Compare the brand, product name, size, UPC and the lot code or best-by date on your package with the recall. Recalls usually cover specific lots or dates, not every package.
- If your product matches, do not eat it. Return it to the store for a refund or throw it away, as the recall notice says.
- If you or someone in your family feels sick after eating a recalled food, call your doctor and say which product it was. Get emergency care for severe symptoms.
- Report a problem or illness to FDA through the Safety Reporting Portal (safetyreporting.hhs.gov). For meat, poultry and egg products, call USDA at 1-888-674-6854.