CLASS I ONGOING Food recall · Reported 29 Jul 2026 · FDA Enforcement Report
Modern Warrior Ready, Dietary Supplement recalled
Modern Warrior Life is recalling Modern Warrior Ready, Dietary Supplement, distributed nationwide in the US. The recall was initiated on 9 Jan 2026 and the FDA has classified it as Class I.
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
- H-1178-2026
- FDA event ID
- 98304
- Recalling firm
- Modern Warrior Life, Scottsdale, AZ
- Brand
- Modern Warrior
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 9 Jan 2026
- FDA classified
- 17 Jul 2026
- Reported
- 29 Jul 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
- Product category
- Dietary Supplements
Timeline
| 9 Jan 2026 | Recall initiated by company | |
| 17 Jul 2026 | Classified by FDA | +189 days |
| 29 Jul 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
Where it was distributed
The recalled product was distributed to customers nationwide from April 2022 until December 8, 2025
Questions about this recall
Why was it recalled?
FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
Which lots are affected?
Product distributed between April of 2022 until December 8th of 2025.
Where was it sold?
The recalled product was distributed to customers nationwide from April 2022 until December 8, 2025
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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.
Other Dietary Supplements recalls
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|---|---|---|---|---|---|
| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
| Food | CLASS I | Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR | ZMB Enterprises | Hidden Drug Ingredients | CA |
| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS II | Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX | Provision Health | Undeclared Allergens | CA |
| Food | CLASS II | Imu-Tek Colostrum recalled by Imu-Tek Animal HealthImu-Tek Colostrum-5 | Imu-Tek Animal Health, Incorporated | Foreign Material | 30 states |