Leader Formulas, LLC. of Tomball, Texas, is recalling one lot of RAPTURE Preworkout dietary supplement powder after FDA testing found the product contains 1,3-Dimethylamylamine (DMAA) — a stimulant drug that the FDA has determined is not a legal dietary supplement ingredient. The recall was announced October 6, 2026. No adverse events have been reported. The product was sold nationwide at retail and online through leaderformulas.com.
What’s Being Recalled?
Three flavors of RAPTURE Preworkout in 450g round plastic containers with red and black lettering are included in lot number 260327-4:
Rainbow Twist — UPC 710154236506
Electric Lemonade — UPC 710143236513
Berry Mojito — UPC 710154236544
The recalled lot was distributed nationwide from January 29, 2025 through May 25, 2026, through retail stores and the company website.
Why Was This Product Recalled?
FDA testing found RAPTURE Preworkout contains DMAA (1,3-Dimethylamylamine), a synthetic stimulant drug that the FDA has determined is not a lawful dietary supplement ingredient and has issued warning letters against since 2012. DMAA can cause elevated blood pressure, cardiovascular problems including heart attack, shortness of breath, and tightening of the chest. DMAA is particularly dangerous when combined with other stimulants such as caffeine — which is commonly found in preworkout supplements. It has been linked to deaths and serious cardiovascular events in military personnel and civilian athletes.
What Should You Do?
Stop using RAPTURE Preworkout immediately if your container has lot number 260327-4. Return it to the place of purchase for a full refund. If you have experienced chest pain, rapid heart rate, shortness of breath, or other cardiovascular symptoms after taking this product, seek medical attention immediately and report the reaction to FDA MedWatch at 1-800-332-1088 or fda.gov/safety/medwatch. Contact Leader Formulas at 832-855-7562, Monday through Friday, 9 a.m. to 5 p.m. CT, or email Patrick@leaderformulas.com.
