FDAClass I · Food · Recall H-1178-2026 · Recalled July 29, 2026

Modern Warrior Ready recall — Modern Warrior Life, LLC

Agency report date: July 29, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Modern Warrior Ready
Company / brand: Modern Warrior Life
Lot / serial / date codes: 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

Agency product description and boundaries

Modern Warrior Ready, Dietary Supplement, 60 CAPSULES

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Modern Warrior Ready

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1178-2026
Brand: Modern Warrior Life
Classification: Class I
Units affected: Unknown
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Modern Warrior Ready

Companies & origin

Recalling firm location: Scottsdale, AZ, United States
Firm address: 6501 E Greenway Pkwy Ste 150, N/A, 85254-2069

Identifying details (verbatim from the notice)

Product codes / lots: 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
Firm notified the public via: Press Release
FDA event ID: 98304
Recall initiated: January 9, 2026
FDA classified: July 17, 2026
FDA report date: July 29, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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