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Safety Reports: Vitamins

Updated:

Real Time Reports

Recall notice

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

2 weeks 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 #dietarysupplements #supplement #unitedstates

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

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

1 month 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 #supplement #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

1 month 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 #supplement #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

Silintan Ache Relief Capsules recalled due to Undeclared Meloxicam, USA

1 month 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 #supplement #dietarysupplements #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

2 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 #supplement #unitedstates

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

Recall notice

Life Magnesium Bisglycinate recalled due to Undeclared Magnesium Oxide, Canada

3 months ago •source recalls-rappels.canada.ca • details

Shoppers Drug Mart and Loblaw Companies Limited have issued a recall for Life Brand Magnesium Bisglycinate 200mg capsules due to the presence of an undeclared ingredient, Magnesium Oxide. The affected products were distributed across Canada.

The recalled product is:
- Life Brand Magnesium Bisglycinate 200mg
- With… See more

#vitamins #supplement #canada

Recalls Life Magnesium Bisglycinate recalled due to Undeclared Magnesium Oxide Shoppers Drug Mart and Loblaw... photo #1
82   Comments Comment

Recall notice

Professional Botanicals Products recalled due to Magnesium Salicylate, United States

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

Professional Botanicals, Inc. has initiated a voluntary recall of three dietary supplements due to the presence of magnesium salicylate, which is not declared on the product labels. The affected products were distributed nationwide in the United States across multiple states, including CA, TX, and NY. A total… See more

#vitamins #supplement #unitedstates #vegetable

Recalls Professional Botanicals Products recalled due to Magnesium Salicylate Professional Botanicals, Inc.... photo #1
24   Comments Comment

Recall notice

SiluetaYa Tejocote Root Dietary Supplement recalled due to Yellow Oleander, USA

4 months ago •source fda.gov • details

SiluetaYa is recalling its tejocote root because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. The tejocote root was distributed online in the United States. The product comes in an 8-ounce container. The recall was the result of sampling conducted… See more

#vitamins #supplement #dietarysupplements #unitedstates

Recalls SiluetaYa Tejocote Root Dietary Supplement recalled due to Yellow Oleander SiluetaYa is recalling it... photo #1
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Recall notice

Multiple Supplements recalled due to Toxic Yellow Oleander, United States

4 months ago •source fda.gov • details

OBC Group Corp and Siluetaya, LLC are recalling certain tejocote root products due to contamination with yellow oleander, a toxic substance. These products were sold online through platforms such as eBay and the Naturalvida website.

The recalled products include:

PRODUCT: SdB Semilla de Brasil Tejocote Root
-… See more

#vitamins #supplement #unitedstates #mexican

Recalls Multiple Supplements recalled due to Toxic Yellow Oleander OBC Group Corp and Siluetaya, LLC are rec... photo #1
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Recall notice

Prazosin Hydrochloride, Capsules recalled due to CGMP deviations, United States

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

Teva Pharmaceuticals USA, Inc. has initiated a voluntary recall of Prazosin Hydrochloride capsules due to CGMP deviations. The recall affects products distributed nationwide in the U.S. due to test results showing impurity levels above acceptable limits. A total of 580,844 bottles are affected.

AFFECTED PRODUCTS:

PRODUCT: Prazosin… See more

#vitamins #recall #supplement #unitedstates

Recalls Prazosin Hydrochloride, Capsules recalled due to CGMP deviations Update October 31st, 2025: The rec... photo #1
23   Comments Comment

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