RECALL RECORD — CLASS IIRecall closedF-0671-2025/FDA enforcement

Omni-macs Mcdonagh Medical Center Dietary Supplement 100 Capsules, Suggested Use: 1-3 Capsules…

What you need to know

Class II
  • What happened

    Levels of iodine exceeding label claim

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDAIN, MOMore supplements

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Product identification

Source: FDA FOOD

Brand nameVeridance Pharmacal, LLC
Recalling firmVeridance Pharmacal, LLCSpringdale, AR, United States
UPC / barcodes
8 50038 22129 4
Lot / date codes
  • UPC: 850038221294, Lot codes: 0311-01 exp. 3/26, 0311-02 exp. 3/26, 0367-01 exp. 8/26
Distribution area
INMO

One customer located in Gladstone, MO

United States

Quantity affected450 bottles
Recall initiationFDA report date: April 2, 2025
FDA recall numberF-0671-2025

Beyond the headline

The recall, in context

Veridance Pharmacal, LLC initiated this supplements recall on March 10, 2025. The FDA enforcement report states: Levels of iodine exceeding label claim. The FDA report lists distribution as: One customer located in Gladstone, MO.

The FDA enforcement report describes the reason as: Levels of iodine exceeding label claim

Omni-macs Mcdonagh Medical Center Dietary Supplement 100 Capsules, Suggested Use: 1-3 Capsules… was made or distributed by Veridance Pharmacal, LLC in Springdale, AR, United States. This page reflects FDA report F-0671-2025, dated April 2, 2025.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Omni-macs Mcdonagh Medical Center Dietary Supplement 100 Capsules, Suggested Use: 1-3 Capsules… recall?

Veridance Pharmacal, LLC recalled Omni-macs Mcdonagh Medical Center Dietary Supplement 100 Capsules, Suggested Use: 1-3 Capsules… in an FDA Class II enforcement action reported as F-0671-2025. Levels of iodine exceeding label claim

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Veridance Pharmacal, LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0671-2025. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.