Full Breakdown
Nationwide Recall of RAPTURE Pre-Workout Powder Over Illegal DMA A Ingredient
By Drooid · · How we work
Core Event
Leader Formulas, LLC of Tomball, Texas announced a voluntary nationwide recall of its RAPTURE pre-workout supplement after testing by the U.S. Food and Drug Administration (FDA) identified the presence of 1,3-dimethylamylamine (DMA A). The recall covers a single lot of the product that was sold in retail stores and through the company’s website between Jan. 29, 2025 and May 25, 2026.
Product Details and Distribution
The recalled lot, identified by number 260327-4, was packaged in 450-gram round plastic containers featuring red and black lettering and a rhinoceros-print seal. Three flavors were affected: Rainbow Twist (UPC 710154236506), Electric Lemonade (UPC 710143236513), and Berry Mojito (UPC 710154236544). All units bearing the specified lot number were distributed nationwide during the stated period.
Regulatory Background on DMA A
DMA A is a synthetic stimulant related to amphetamine that was once used as a nasal decongestant but was withdrawn from the market in the 1980s. The Department of Defense notes that the FDA has classified DMA A-containing dietary supplements as illegal since 2013, and the agency has repeatedly warned that such products can raise blood pressure and trigger cardiovascular problems, including heart attack, shortness of breath, and chest tightness.
Official Actions and Consumer Guidance
Leader Formulas is notifying distributors and customers by mail, arranging for the return of all recalled units, and offering full refunds to purchasers. The company has reported no adverse health events linked to the recalled products as of early October 2026. The FDA advises anyone who has purchased the RAPTURE pre-workout to stop using it, return it to the place of purchase, and report any health concerns through its Safety Reporting Portal.
Impact and Next Steps
Consumers with the recalled product are urged to follow the return instructions to obtain refunds and to avoid further consumption. Health authorities continue to monitor the situation, emphasizing that DMA A has no recognized medical use and remains prohibited in dietary supplements across the United States and several other countries.