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Leader Formulas, LLC, is recalling one lot of RAPTURE Preworkout powder after FDA testing found 1,3-dimethylamylamine (DMAA) in the product. The company says the lot was distributed nationwide from January 29, 2025, through May 25, 2026, and advises consumers to stop using it and return it for a full refund.
Leader Formulas, LLC, is recalling one lot of its RAPTURE Preworkout dietary supplement powder nationwide after testing by the U.S. Food and Drug Administration found 1,3-dimethylamylamine (DMAA), the company said in a recall announcement dated October 6. The FDA posted the company’s notice on October 7. Consumers who have the affected product are advised to stop using it and return it to the place of purchase for a full refund.
The recall covers product with lot number 260327-4. RAPTURE Preworkout is sold in 450-gram round plastic containers with red and black lettering and a rhinoceros image on the seal. The notice lists three affected flavors: Rainbow Twist, Electric Lemonade and Berry Mojito. Their UPCs are 710154236506, 710143236513 and 710154236544, respectively.
Leader Formulas, based in Tomball, Texas, said the affected product was distributed nationwide to retail outlets and through its website, leaderformulas.com, from January 29, 2025, through May 25, 2026. The company said it is notifying distributors and customers by mail and arranging for recalled products to be returned. It advises consumers to take the product back to where they bought it for a full refund.
The company announcement says DMAA use can raise 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 reports of adverse events related to the recall at the time of the notice. The FDA says the recall is being conducted with its knowledge; its posting of a company announcement is a public service and does not mean the agency endorses the product or company.
Risks and Consumer Steps
The recall matters to people who bought or may still have lot 260327-4, because the company says the product contains DMAA and recommends that consumers stop using it. The notice identifies possible cardiovascular effects associated with DMAA use, so anyone who has used the product and is experiencing health problems should contact a physician or other healthcare provider, as the company advises.
The distribution period extended across more than a year and included both retail sales and online orders, according to the announcement. That means consumers may need to check the lot number and flavor on containers they already own rather than rely only on when or where they bought them. The company’s full-refund instruction gives affected buyers a stated next step, while the notice does not describe a replacement product or a different remedy.
The announcement reports no adverse-event complaints received by the company, but that statement does not establish that no one experienced symptoms. Consumers can report adverse reactions or product-quality problems to the FDA’s MedWatch program. The notice lists online reporting, mail and fax as options.
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How the Recall Was Identified
The notice identifies FDA testing as the way the issue was found. It does not give the testing date, explain how many samples were tested, or state how much DMAA was detected. The recall is described as voluntary and covers one specified lot, rather than every RAPTURE product or every lot of the product.
The FDA page labels its posting a company announcement. It explains that the agency shares recall notices as a public service and does not endorse the company or product by posting them. The company says the recall is being conducted with FDA’s knowledge, but the supplied notice does not describe any separate FDA enforcement action.
““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 company recall announcement
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Details Not Given in Notice
The notice does not state how much DMAA was found, how many containers are affected, or how many have been sold or returned. It also does not provide a test date or additional information about the testing method. Those details are not available in the supplied announcement.
It is also unclear whether the company or FDA has identified other lots or products with the same issue. The company’s report of no adverse-event reports is limited to what it had received at the time; the notice does not provide an independent count of possible consumer symptoms. Further updates could clarify the scale of the recall, but none are specified in the announcement.
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Refunds and FDA Reports
Consumers who identify the affected lot should stop using the powder and return it to the place of purchase for a full refund. People with questions can contact Leader Formulas 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.
Anyone who experiences a problem they believe may be related to using the product should contact a physician or healthcare provider, according to the company’s notice. Adverse reactions or product-quality issues can also be reported to FDA MedWatch online at fda.gov/medwatch/report.htm, by fax at 1-800-FDA-0178, or by mail using a MedWatch form. The announcement gives no date for completion of the returns or for any further recall update.
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Key Questions
Which RAPTURE Preworkout products are included in the recall?
The recall covers lot 260327-4 of RAPTURE Preworkout powder. The notice lists Rainbow Twist (UPC 710154236506), Electric Lemonade (UPC 710143236513) and Berry Mojito (UPC 710154236544). Check the lot number and UPC on the container.
What should I do if I have the affected product?
Stop using it and return it to the place of purchase for a full refund, as Leader Formulas advises. Contact the company if you have questions about the recall or return process.
Why is RAPTURE Preworkout being recalled?
Leader Formulas says FDA testing found 1,3-dimethylamylamine (DMAA) in the product. The company notice says DMAA use can raise blood pressure and could lead to cardiovascular problems, including heart attack, shortness of breath and chest tightness.
Were any adverse events reported?
Leader Formulas said it had received no reports of adverse events related to the recall when it issued the announcement. That statement does not confirm that no consumers experienced symptoms. People with health concerns should contact a healthcare provider and may report suspected reactions to FDA MedWatch.
Where can I ask questions or report a problem?
Leader Formulas lists Patrick@leaderformulas.com and 832-855-7562 for consumer questions, Monday through Friday, 9 a.m. to 5 p.m. Central Time. Suspected adverse reactions or product-quality problems can be reported to FDA MedWatch online, by mail or by fax.
Source: primary
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