MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement, 60 Capsule Bottle (30 Serving). Manufactured exclusively f
Summary
The FDA issued a Class II for MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement, 60 Capsule Bottle ( by MTN OPS, LLC. Reason: Undeclared soy flour.
Details
Source
Food Recall
External ID
F-0698-2025
Action Date
2025-04-16
Status
Terminated
Category
food
Product Description
MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement, 60 Capsule Bottle (30 Serving). Manufactured exclusively for MTN OPS, LLC, 251 S Mountain Rd., Fruit Heights, UT. UPC 8 40359 40458 2
Lot/Code Info: Expiration Date: 03/2026, Lot# 012324177
Quantity Affected: 7546 bottles
Reason for Recall
Undeclared soy flour
Distribution
Distributed nationwide except RI and distributed in Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-25
Company
Fruit Heights, UT
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (MTN OPS, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MTN OPS, LLC have FDA actions?
This is the only FDA action we have on record for MTN OPS, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0698-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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