UnratedFood recall · FDA · Published January 9, 2026
Modern Warrior Dietary Supplement Recall: Unapproved Ingredients Found
Modern Warrior recalls 60-capsule dietary supplement sold from April 2022 to December 2025 due to FDA-detected unapproved ingredients including tianeptine and DMAA.
“Modern Warrior Dietary Supplement Recall: Unapproved Ingredients Found.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/84584-modern-warrior-dietary-supplement-recall-unapproved-ingredients-found. Based on FDA recall #H-1178-2026.
The Food and Drug Administration announced on Jan. 9, 2026, that Modern Warrior Life, LLC voluntarily recalled Modern Warrior Ready dietary supplement because FDA analysis revealed unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
How to tell if you have it
Brand: Modern Warrior
Product: Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
Distribution: Nationwide from April 2022 until December 8, 2025
The hazard
FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
Context
GovInfoNow's records show other recent recalls of similar products include Sinus Cap Herbal Supplement Recall: Unapproved Drug Claims on Label (2025-11-20), Pain Away Herbal Supplement Recall: Unapproved Drug Claims on Label (2025-11-20), and A New Life Herbs Chaga Mushroom Supplement: Unapproved Health Claims (2025-11-20).
How to tell if you have this one
Check for the product name 'Modern Warrior Ready' and the number of capsules (60). The product was sold from April 2022 through December 2025.
Brand
Modern Warrior
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the product name 'Modern Warrior Ready' and the number of capsules (60) to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “The recalled product was distributed to customers nationwide from April 2022 until December 8, 2025” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 7 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-1178-2026 (January 9, 2026)
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.