Multivitamin recall FDA

A voluntary recall has been issued for a popular brand of men’s multivitamins due to the unexpected presence of an undeclared allergen, posing a potential health risk to individuals with soy sensitivities.

MTN OPS LLC, a company located in Utah, is conducting the recall affecting their “Multi-V Men” multivitamin. The recall encompasses approximately 7,546 bottles containing 60 capsules each.

The Food and Drug Administration (FDA) initiated this action on April 9th due to the detection of “undeclared soy flour” within the product. This ingredient was not listed on the label, potentially causing a severe reaction in those with allergies.

The FDA has classified this recall as Class II. According to the agency, this designation applies to situations where “temporary or medically reversible adverse health consequences” may occur, although the probability of serious harm is considered low.

Bottles subject to the recall are marked with an expiration date of March 2026 and bear lot number #012324177. MTN OPS has confirmed that only this specific batch is affected, and other production runs remain unaffected.

These multivitamins are formulated to provide essential nutrients crucial for male health and well-being. The formula includes:

  • Calcium
  • Zinc
  • Vitamin C
  • Vitamin B-12
  • Vitamin D
  • Thiamin

The company markets the product as a way to support “daily health” and “immune health,” stating on their website:

“Men need specific nutrients to maintain optimal health. Men’s Multi-V is a daily multivitamin with essential vitamins and minerals you need to maintain a strong, healthy, and energetic lifestyle.”

Recalls of over-the-counter medications and supplements are infrequent but do occur. Past instances include a 2016 recall by Nature Made due to concerns about potential contamination with salmonella or staphylococcus, and a more recent November recall of clonazepam, an anti-anxiety medication, stemming from labeling errors.

MTN OPS LLC has not yet responded to requests for comment regarding this voluntary recall.

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