Food recall

Veridance Pharmacal, LLC recall: Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use

Veridance Pharmacal, LLC, of Springdale, AR, recalled Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use. The FDA's reason: “Levels of iodine exceeding label claim.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on March 10, 2025, and the FDA first listed it in its Enforcement Report of April 2, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Labeling, packaging or manufacturing problems

Status

Terminated

Closed April 4, 2025

The recall

Company
Veridance Pharmacal, LLC (Springdale, AR)
Reason, in FDA's words
“Levels of iodine exceeding label claim”
Where it was sold
One customer located in Gladstone, MO
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
96473

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0671-2025 Class II

    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

    Codes: UPC: 850038221294, Lot codes: 0311-01 exp. 3/26, 0311-02 exp. 3/26, 0367-01 exp. 8/26

    Quantity: 450 bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of April 2, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.