The U.S. Food and Drug Administration (FDA) has assigned its highest risk ranking to all lots of a mental clarity supplement sold nationwide online.
The recalled supplements were distributed to customers nationwide from April 2022 until Dec. 8, 2025, by Modern Warrior Life of Scottsdale, Arizona.
The FDA notes on its website that tianeptine can cause life-threatening events including suicidal ideation or behavior in children, adolescents, and adults aged 25 years and younger and that using tianeptine with monoamine oxidase inhibitor antidepressants could lead to life-threatening complications including stroke and death.
The FDA further states that use of 1,4-DMAA can elevate blood pressure and lead to cardiovascular problems, including heart attack, shortness of breath, and tightening of the chest, while products containing synephrine can potentially result in increased heart rate and blood pressure, especially in the presence of caffeine.
Modern Warrior Life management did not respond to requests for comment by the time of publication.
The original recall was announced in January. Since the recall was initially publicized, the FDA assigned the dietary aid its highest risk warning at Class 1.
A Class 1 event is defined on the FDA website as having a reasonable probability that the use of or exposure to will cause serious adverse health consequences or death, while Class 2 signals that the risk is temporary or adverse health consequences are medically reversible.
A Class 3 label involves products that violate regulations but are unlikely to cause health problems, such as minor labeling errors.
Prior to its recall, Modern Warrior Life sold the Ready product for $169.99 as part of a 3-step Body Repair Plan, known as BRP, which included two other supplements called Reset and Realign.
Purchasing of the BRP product containing Ready supplements is no longer enabled on the Modern Warrior Life website.