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Leader Formulas, LLC, is voluntarily recalling one lot of RAPTURE Preworkout dietary supplement powder after FDA testing found DMAA in the product. The affected lot, 260327-4, was distributed nationwide from January 29, 2025, to May 25, 2026; the company says it has received no reports of related adverse events.
Leader Formulas, LLC is voluntarily recalling one lot of its RAPTURE Preworkout dietary supplement powder after testing by the U.S. Food and Drug Administration found 1,3-dimethylamylamine (DMAA) in the product. The affected lot was sold nationwide, and the company advises consumers to stop using it and return it to the place of purchase for a full refund.
The recall covers products marked with lot number 260327-4. The powder is packaged in 450-gram round plastic containers with red and black lettering and a rhinoceros image on the seal. The company identifies three affected flavors and UPCs: Rainbow Twist, 710154236506; Electric Lemonade, 710143236513; and Berry Mojito, 710154236544.
According to the company announcement posted by the FDA, the product was distributed from January 29, 2025, through May 25, 2026, both to retail outlets and online through Leader Formulas’ website. The company said it is notifying distributors and customers by mail and arranging for recalled products to be returned. Consumers who bought the affected product are advised to stop using it and return it to the place of purchase for a full refund.
The announcement says DMAA use can raise blood pressure and could lead to cardiovascular problems, including heart attack, shortness of breath and chest tightening. Leader Formulas reported that it had received no reports of adverse events related to the recall at the time of its 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 Returns
The recall affects a product sold to consumers across the country over a period of more than a year, including through online sales. Identifying the lot number, flavor and UPC lets customers check whether a container they bought is included, while the return instructions provide a route to a refund.
The health concern named in the announcement is the presence of DMAA. The company’s notice warns of possible elevated blood pressure and cardiovascular effects; it does not say that every consumer who used the powder will experience harm. The reported absence of adverse-event reports is the company’s statement as of the notice, not evidence that the product is risk-free. Anyone who believes they have experienced a problem after using the product is advised to contact a physician or other healthcare provider.
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How the Recall Was Identified
The FDA page labels this a company announcement and says it posts recall, market-withdrawal and safety-alert notices as a public service. The agency also states that publication does not mean it endorses the product or the company. The recall announcement says the issue was identified when the FDA tested the product.
Leader Formulas, based in Tomball, Texas, described the action as a voluntary recall and said it was being conducted with the FDA’s knowledge. The notice does not describe the testing method or provide laboratory results. Its central consumer instruction is specific to the listed lot: stop using the affected product and seek a refund from the place of purchase.
“The issue was discovered in the product during testing by the FDA.”
— Leader Formulas, LLC, in the recall announcement posted by the FDA
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Details Not Provided in the Notice
The announcement does not give the amount or concentration of DMAA found in the product, explain how many containers were distributed, or describe the testing procedures or results beyond stating that FDA testing identified the substance. It also does not specify how many customers or retail locations received the affected lot.
The company reported no related adverse-event reports, but the notice does not provide a separate FDA assessment of consumer effects or say whether additional lots or products were tested. The scope stated in the announcement is one lot, number 260327-4; whether any broader action will follow is not addressed.
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Returns and Safety Reports
Leader Formulas said it is contacting distributors and customers by mail and arranging for returns. Consumers should check the container against lot 260327-4 and the listed product details, stop using it if it matches, and contact the place of purchase about a full refund. Questions can be directed to the company by email at Patrick@leaderformulas.com or by phone at 832-855-7562 during the stated weekday hours.
People who think they have experienced a problem related to using the product should contact a physician or healthcare provider, according to the notice. Adverse reactions or product-quality concerns can also be reported to the FDA’s MedWatch program online or by mail or fax using the agency’s reporting forms. The announcement does not state a deadline for returns or give a date for further updates.
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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 announcement lists Rainbow Twist (UPC 710154236506), Electric Lemonade (UPC 710143236513) and Berry Mojito (UPC 710154236544).
Why is the product being recalled?
Leader Formulas says FDA testing found DMAA in the product. The company announcement warns that DMAA can raise blood pressure and could lead to cardiovascular problems.
What should consumers do if they have the affected lot?
Consumers should stop using the product and return it to the place of purchase for a full refund, according to the company. They can contact Leader Formulas at Patrick@leaderformulas.com or 832-855-7562, Monday through Friday, 9 a.m. to 5 p.m. Central Time.
Have any adverse events been reported?
Leader Formulas said it had received no reports of related adverse events when it issued the recall announcement. The notice does not provide independent case data or establish whether any consumers have experienced symptoms.
When and where was the product sold?
The affected product was distributed nationwide from January 29, 2025, to May 25, 2026, through retail outlets and the company website, according to the announcement.
Source: primary
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