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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Latest Posted April 10, 2025
MTM OPS Men’s Multivitamin Recalled
On April 9, 2025, MTN OPS, LLC recalled 7,546 bottles of MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement because it contains undeclared soy flour.
People with an allergy to soy should not consume these products as they could cause a serious or life-threatening allergic reaction.
(See ConsumerLab’s Multivitamin and Multimineral Review for tests of related products.)
Recalled MTN OPS MULTI-V Men's Daily Multivitamins were sold nationwide in the U.S. except for in Rhode Island and distributed in Canada. They can further be identified by the following:
- Product name: MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement
- Packaging: 60 Capsule Bottle (30 Serving)
- UPC: 8 40359 40458 2
- Expiration Date: 03/2026
- Lot number: 012324177
MTN OPS, LLC is notifying consignees or the public of the recall by email.
For more information, use the link below.
Enforcement Report: MTN OPS MULTI-V Men's Daily Multivitamin
See related recalls and warnings:
Flaxseed Oil Recalled Due to Undeclared Allergen
Sleep Supplement Recalled Due to Undeclared Soy
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
Dietary Supplement or Nutritional Product Problem Report
If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
Please complete the form below as accurately as possible. You may need to check the label on the product.
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Generic Drug Problem Report
If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
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Other Recent Recalls & Warnings
For information about reporting serious reactions and problems with medical products to the U.S. Food and Drug Administration through its MedWatch reporting program, please visit the FDA MedWatch website.
