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Leader Formulas, LLC. is voluntarily recalling one lot of RAPTURE Preworkout after FDA testing found 1,3-dimethylamylamine (DMAA) in the dietary supplement powder. The affected lot is 260327-4; the company says it has received no reports of adverse events and advises consumers to stop using the product and seek a full refund from the place of purchase.
Leader Formulas, LLC. has issued a voluntary nationwide recall of one lot of its RAPTURE Preworkout dietary supplement after testing by the U.S. Food and Drug Administration found 1,3-dimethylamylamine (DMAA) in the powder. The company says consumers who bought the affected product should stop using it and return it to the place of purchase for a full refund; DMAA use can raise blood pressure and may lead to serious cardiovascular problems.
The recalled product is RAPTURE Preworkout lot 260327-4, sold in 450-gram round plastic containers with red and black lettering and a rhinoceros print seal on top. The announcement identifies three flavors: Rainbow Twist (UPC 710154236506), Electric Lemonade (UPC 710143236513), and Berry Mojito (UPC 710154236544). Consumers should check the lot number as well as the product name and packaging when determining whether their container is included.
Leader Formulas, based in Tomball, Texas, said the affected products were distributed nationwide from January 29, 2025, through May 25, 2026, to retailers and online through the company website. The company is notifying distributors and customers by mail and arranging for recalled products to be returned. It says the recall is being conducted with the knowledge of the FDA; the agency’s posting of a company announcement does not mean it endorses the company or product.
The company announcement says DMAA can cause elevated blood pressure and could lead to cardiovascular problems, including heart attack, shortness of breath and chest tightness. Leader Formulas reported that it had received no adverse-event reports related to the recall as of the announcement. Consumers with questions can contact the company at Patrick@leaderformulas.com or 832-855-7562, Monday through Friday, 9 a.m. to 5 p.m. Central Time.
Health Risks and Consumer Steps
The recall matters because the affected product is a dietary supplement powder sold nationwide, and the FDA testing cited in the company notice found DMAA in the identified lot. The notice describes potential effects that include increased blood pressure and cardiovascular problems. Consumers who have a container from the recalled lot should not keep taking it while they seek a refund.
The company’s statement that it has received no reports of adverse events is a report about what it has received, not evidence that no one experienced symptoms. Anyone who believes they have had a health problem after using the product should contact a physician or healthcare provider. The FDA also accepts reports of adverse reactions or product-quality concerns through its MedWatch program.
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How the Recall Was Identified
According to the company announcement posted by the FDA, the issue was identified when the product was tested by the FDA. Leader Formulas then announced a voluntary recall covering one lot rather than all RAPTURE Preworkout products. The announcement was dated October 6, 2026, and the FDA published it the following day as a public service.
The FDA page says that it posts company announcements about recalls, market withdrawals and safety alerts, and that posting does not constitute an endorsement of the product or company. The stated distribution period—January 29, 2025, to May 25, 2026—means affected containers may have been sold through both retail and online channels over more than a year. The lot number, flavor and UPC details in the notice help consumers identify the specific products covered.
“Consumers who have purchased the RAPTURE Preworkout products which are being recalled should stop using the products and return to the place of purchase for a full refund.”
— Leader Formulas, LLC., in its recall announcement
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Open Questions About Affected Products
The announcement identifies one lot, 260327-4, but does not state how many containers were distributed, how many have been returned, or how many may remain with consumers or retailers. It also does not give a testing result showing the amount of DMAA detected. The notice says the issue was found during FDA testing but provides no further details about the test or when it occurred.
Leader Formulas reported no adverse-event reports as of its announcement, but the notice does not establish whether consumers experienced symptoms that were not reported to the company. The available information also does not say when the company expects the returns process to be completed or whether additional lots or products are under review.
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Returns and Safety Reporting
Consumers with the affected lot number should stop using the product and return it to the place of purchase for a full refund, according to Leader Formulas. People unsure whether their container is covered can contact the company by email at Patrick@leaderformulas.com or by phone at 832-855-7562, Monday through Friday, 9 a.m. to 5 p.m. Central Time. The company says it is notifying distributors and customers by mail and arranging returns.
Anyone who has experienced a problem they believe may be related to using the product should contact a physician or healthcare provider. Adverse reactions or quality concerns may also be submitted to the FDA through MedWatch, online at www.fda.gov/medwatch/report.htm, or by mail or fax using the FDA’s reporting form. The announcement does not provide a timeline for further updates; consumers can check the FDA recall notice or contact Leader Formulas for current return information.
preworkout with cardiovascular risks
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Key Questions
Which RAPTURE Preworkout products are included in the recall?
The recall covers lot 260327-4 of RAPTURE Preworkout in Rainbow Twist (UPC 710154236506), Electric Lemonade (UPC 710143236513) and Berry Mojito (UPC 710154236544). The affected product is described as powder in a 450-gram round plastic container with red and black lettering and a rhinoceros print seal.
Why is RAPTURE Preworkout being recalled?
Leader Formulas said FDA testing found DMAA in the affected lot. The company’s announcement says DMAA can raise blood pressure and could lead to cardiovascular problems, including heart attack, shortness of breath and chest tightness.
What should I do if I have the recalled product?
Stop using it and return it to the place of purchase for a full refund, according to the company. For questions about the recall, contact Leader Formulas at Patrick@leaderformulas.com or 832-855-7562 during its stated weekday business hours.
Have any adverse events been reported?
Leader Formulas said it had received no reports of adverse events related to the recall when it issued its announcement. That statement does not confirm whether any unreported reactions occurred. People who think they have experienced a problem should contact a healthcare provider and may also report it to the FDA’s MedWatch program.
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