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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Omni-Macs Dietary Supplements Recalled for Excessive Iodine Levels

Agency Publication Date: March 27, 2025
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Summary

Veridance Pharmacal, LLC has recalled 450 bottles of Omni-Macs McDonagh Medical Center Dietary Supplement because the product contains iodine levels that exceed the amount listed on the label. The recall affects 100-capsule bottles with a suggested use of 1-3 capsules per day. No incidents or injuries have been reported to date, and the distribution was limited to a single customer in Gladstone, Missouri.

Risk

Consuming excessive levels of iodine beyond what is stated on a label can lead to thyroid dysfunction or other adverse health effects, particularly in sensitive populations.

What You Should Do

  1. The recalled products are 100-capsule bottles of Omni-Macs McDonagh Medical Center Dietary Supplement with UPC 850038221294.
  2. Check the bottle for lot codes 0311-01 (exp. 3/26), 0311-02 (exp. 3/26), or 0367-01 (exp. 8/26) to see if your supplement is part of the recall.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Omni-Macs McDonagh Medical Center Dietary Supplement (100 CAPSULES)by Omni-Macs
Variants: 100 CAPSULES
UPC Codes:
850038221294
Lot Numbers:
0311-01 (exp. 3/26)
0311-02 (exp. 3/26)
0367-01 (exp. 8/26)

Suggested Use: 1-3 capsules per day with meals. Distributed to one customer located in Gladstone, MO.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96473
Status: Resolved
Manufacturer: Veridance Pharmacal, LLC
Sold By: McDonagh Medical Center
Manufactured In: United States
Units Affected: 450 bottles
Distributed To: Missouri

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.