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Supplement Reports

Reports of supplement-related side effects, contamination, and recalls. Browse reports below.

Vitamins Protein Probiotics Greens Powders Wellness Coffee Meal Shakes Gummies

Real Time Reports

Recall notice

Alkaloids Chewable Tablets - White Vein recalled due to Elevated Level of 7-OH, USA

1 month ago •source fda.gov • details

Uodate March 18th, 2026:
The recall was classified as Class I.

Source: www.accessdata.fda.gov/scripts/ires/index.cfm


February 17th, 2026:
Shaman Botanicals, LLC is voluntarily recalling one lot (Lot B# AAW.501.3) of Alkaloids Chewable Tablets—White Vein to the consumer level. Recent testing showed that the Alkaloids Chewable Tablets—White Vein product contains… See more

#gummies #recall #unitedstates

Recalls Alkaloids Chewable Tablets - White Vein recalled due to Elevated Level of 7-OH Uodate March 18th, 20... photo #1
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Recall notice

Green Lumber Dietary Supplement recalled due to Undeclared prescription drug-Tadalafil, USA

1 month ago •source fda.gov • details

Green Lumber Holding, LLC ("Green Lumber") is issuing an updated consumer alert regarding counterfeit products falsely marketed as genuine Green Lumber products that may pose potential health risks. The affected product is distributed nationwide in the United States.

This update follows the U.S. Food and Drug Administration's… See more

#vitamins #unitedstates

Recalls Green Lumber Dietary Supplement recalled due to Undeclared prescription drug-Tadalafil Green Lumber... photo #1
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Recall notice

Aonic Complete His/Her recalled due to E. Coli Contamination, Utah, United States

1 month ago •source accessdata.fda.gov • details

Update February 20th, 2026:
The FDA has updated the recall classification for both Aonic Complete Hers and Aonic Complete His dietary supplement drink shots to Class II. Minor administrative updates were also made to the product descriptions and code formatting.

The affected lot codes remain:
- Lot… See more

#greenspowders #utah #unitedstates

Recalls Aonic Complete His/Her recalled due to E. Coli Contamination Update February 20th, 2026: The FDA h... photo #1
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Recall notice

Imu-Tek Immuno-5 Colostrum Powder recalled due to Undeclared Allergen, United States

2 months ago •source accessdata.fda.gov • details

Imu-Tek Animal Health, Incorporated has initiated a voluntary recall of its Immuno-5 Colostrum Powder due to an undeclared milk allergen. The product was distributed across several states, including AZ, CA, CO, FL, MA, ME, MN, NC, NH, OK, RI, TN, TX, UT, and WI in the United… See more

#milkallergy #mealshakes #unitedstates #milk

Recalls Imu-Tek Immuno-5 Colostrum Powder recalled due to Undeclared Allergen Imu-Tek Animal Health, Incorpo... photo #1
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Recall notice

OptiWize Health OptiWize Collagen Plus recalled due to Mislabeling, United States

2 months ago •source accessdata.fda.gov • details

Optiwize Inc. has initiated a voluntary recall of its OptiWize Collagen Plus due to discrepancies in labeled ingredient quantities. The labeled ingredient quantities did not align with analytical test results. The product was distributed nationwide in the United States via the Amazon website. Testing revealed that the… See more

#protein #unitedstates

Recalls OptiWize Health OptiWize Collagen Plus recalled due to Mislabeling Optiwize Inc. has initiated a vol... photo #1
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Recall notice

Qunol, Extra Strength Turmeric Capsule recalled due to Mold Contamination, United States

2 months ago •source accessdata.fda.gov • details

Update January 29th, 2026:
Wegmans Food Markets has issued a related retail recall notice for select Qunol turmeric supplements sold specifically at Wegmans locations.

According to Wegmans, the affected products include:

PRODUCT: Qunol Turmeric High Absorption Supplement 1000mg
- 60-count
- UPC 8-50184-00842-8
- Lot Code 12811C60… See more

#vitamins #mold #recall #unitedstates

Recalls Qunol, Extra Strength Turmeric Capsule recalled due to Mold Contamination Update January 29th, 2026:... photo #1
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Recall notice

Ready Dietary Supplement recalled due to Undeclared Drug Ingredients, USA

2 months ago •source fda.gov • details

Modern Warrior is voluntarily recalling all lots of Modern Warrior Ready, a dietary supplement sold directly to consumers, after regulatory testing identified the presence of undeclared ingredients, including tianeptine, 1,4-DMAA, and aniracetam. The recalled product was distributed to customers nationwide in the United States from April 2022… See more

#vitamins #recall #unitedstates

Recalls Ready Dietary Supplement recalled due to Undeclared Drug Ingredients Modern Warrior is voluntarily r... photo #1
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Recall notice

HerbsForever Dietary Supplements recalled due to Undeclared Allergen, USA

2 months ago •source fda.gov • details

Update January 14th, 2026:
The recall was classified as Class I.

Source: www.accessdata.fda.gov/scripts/ires/index.cfm


January 9th, 2026:
HerbsForever LLC of Los Angeles, California, is recalling 45 units of the product “Hingwastik Churna” and 45 units of “Gastro Care” dietary supplements because they may contain undeclared wheat. People who… See more

#probiotics #wheatallergy #unitedstates

Recalls HerbsForever Dietary Supplements recalled due to Undeclared Allergen Update January 14th, 2026: Th... photo #1
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Recall notice

Silintan Ache Relief Capsules recalled due to Undeclared Meloxicam, USA

2 months ago •source fda.gov • details

ANTHONY TRINH, 123herbals LLC is voluntarily recalling all lots of Silintan capsules to the consumer level. FDA analysis has found the product to be tainted with meloxicam. Meloxicam, is an approved Nonsteroidal Anti-Inflammatory Drug, (NSAID) indicated for management of osteoarthritis pain. Products containing meloxicam cannot be marketed… See more

#vitamins #recall #unitedstates

Recalls Silintan Ache Relief Capsules recalled due to Undeclared Meloxicam ANTHONY TRINH, 123herbals LLC is... photo #1
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Recall notice

Male Enhancement Dietary supplement recalled due to Undeclared Sildenafil and Tadalafil, USA

3 months ago •source fda.gov • details

StuffbyNainax LLC is voluntarily recalling all lots of MR.7 SUPER 700000 capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil and tadalafil, which are active ingredients in FDA-approved prescription drugs used to treat male erectile dysfunction and belong to a… See more

#vitamins #recall #unitedstates

Recalls Male Enhancement Dietary supplement recalled due to Undeclared Sildenafil and Tadalafil StuffbyNaina... photo #1
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