CLASS II Food recall · Reported 16 Apr 2025 · FDA Enforcement Report
Multi-v Men's Daily Multivitamin dietary supplement recalled by Mtn Ops
Mtn Ops is recalling Multi-v Men's Daily Multivitamin dietary supplement, distributed nationwide in the US. The recall was initiated on 25 Mar 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0698-2025
- FDA event ID
- 96578
- Recalling firm
- Mtn Ops, Fruit Heights, UT
- Brand
- Mtn Ops
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 25 Mar 2025
- FDA classified
- 9 Apr 2025
- Reported
- 16 Apr 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Soy
- Product category
- Vitamins
Timeline
| 25 Mar 2025 | Recall initiated by company | |
| 9 Apr 2025 | Classified by FDA | +15 days |
| 16 Apr 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared soy flour
Product as listed by the FDA
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
Where it was distributed
Distributed nationwide except RI and distributed in Canada
Questions about this recall
Why was it recalled?
Undeclared soy flour
Which lots are affected?
Expiration Date: 03/2026, Lot# 012324177
Where was it sold?
Distributed nationwide except RI and distributed in Canada
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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