Modern Warrior Life, LLC Recall: FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
United States
OngoingClass I
- Company
- Modern Warrior Life, LLC
- Product
- Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
- Recall date
- January 9, 2026
- Source
- FDA
Reason for recall
FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Modern Warrior Ready, Dietary Supplement, 60 CAPSULES | Not published in this source record | Unknown | Product distributed between April of 2022 until December 8th of 2025. |
Distribution
- The recalled product was distributed to customers nationwide from April 2022 until December 8
- 2025
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-1178-2026
- Event ID
- 98304
- Status
- Ongoing
- Classification
- Class I
- Company
- Modern Warrior Life, LLC
- Product description
- Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
- Quantity
- Unknown
- Reason
- FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
- Recall initiation date
- January 9, 2026
- Report date
- July 29, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- The recalled product was distributed to customers nationwide from April 2022 until December 8, 2025
- UPC, lot, and code information
- Product distributed between April of 2022 until December 8th of 2025.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Modern Warrior Life, LLC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
