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Leader Formulas, LLC, is voluntarily recalling lot 260327-4 of RAPTURE Preworkout powder after FDA testing found 1,3-dimethylamylamine (DMAA). The company says the product was sold nationwide from Jan. 29, 2025, through May 25, 2026, and advises consumers to stop using it and return it for a full refund.
Leader Formulas, LLC, is voluntarily 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) in the product. The company says consumers who bought the affected lot should 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. RAPTURE Preworkout is sold in 450-gram round plastic containers with red and black lettering and a rhinoceros-print seal on top. The listed flavors are Rainbow Twist, Electric Lemonade and Berry Mojito; the announcement provides UPCs for each flavor as product identifiers.
Leader Formulas, based in Tomball, Texas, says the affected products were distributed nationwide to retail outlets and through its website from Jan. 29, 2025, to May 25, 2026. The company says it is notifying distributors and customers by mail and arranging for recalled products to be returned. Consumers are instructed to stop using the product and take it back to the place of purchase 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 reports that it has received no reports of adverse events related to the recall. That statement describes reports received by the company; it does not establish whether any unreported effects occurred.
Health Risks and Consumer Refunds
The recall concerns a supplement that consumers may have bought for use around exercise, and the identified ingredient is associated in the company’s announcement with potential blood-pressure and cardiovascular risks. People who have the specified lot should not continue taking it while the recall is in effect, even if they have not noticed symptoms. The announcement does not say that every container or every lot of RAPTURE Preworkout is affected; it identifies lot 260327-4.
The broad distribution period and nationwide reach mean the product may have been purchased both from stores and online. Checking the lot number and product details can help consumers determine whether their container is part of the recall. Anyone who experiences a problem they believe may be related to use should contact a physician or other healthcare provider, as the company advises, and may report an adverse event to FDA’s MedWatch program.
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How the Recall Was Triggered
The FDA notice is identified as a company announcement posted by the agency as a public service. The notice says FDA does not endorse the product or the company. According to Leader Formulas, the issue was discovered when the product was tested by the FDA, after which the company initiated a voluntary recall with FDA’s knowledge.
The recall notice identifies a specific lot rather than describing a recall of all RAPTURE products. Its product identifiers include the container size and packaging, the lot number, three flavor names, and corresponding UPCs. Consumers should compare the information on their container with the official recall notice rather than relying on flavor or packaging alone.
““The issue was discovered in the product during testing by the FDA.””
— Leader Formulas, LLC, in its recall announcement
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Scope and Health Reports
The notice specifies one affected lot, but does not state how many containers were distributed or how many have been returned. It also does not provide details about the amount or concentration of DMAA detected, the testing method, or whether additional testing is underway. The company’s statement that it has received no adverse-event reports is not the same as confirmation that no consumer experienced a problem.
The announcement does not identify specific retailers or provide information on how many customers have been reached by the company’s mail notifications. It remains unclear how many recalled containers may still be held by consumers or retailers. The listed distribution dates describe when the affected product was distributed, not how long any individual container remains available for purchase.
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Returns and Consumer Reporting
Leader Formulas says it is contacting distributors and customers by mail and arranging returns of recalled products. Consumers with lot 260327-4 should stop using the powder and contact the place of purchase about the full refund. Questions may be directed to the company at Patrick@leaderformulas.com or 832-855-7562, Monday through Friday, 9 a.m. to 5 p.m. Central time.
People who believe they have experienced a problem after using the product should contact a healthcare provider. The company’s notice also directs consumers to report adverse reactions or product-quality concerns to the FDA’s MedWatch Adverse Event Reporting program, online, by mail or by fax. The notice does not give a deadline for returns or say when the recall process will be complete.
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Key Questions
Which RAPTURE Preworkout product is being recalled?
The recall covers lot 260327-4 of RAPTURE Preworkout powder in 450-gram containers. The notice lists Rainbow Twist, Electric Lemonade and Berry Mojito and provides a UPC for each flavor. Check the lot number and product details against the recall announcement.
Why is the product being recalled?
Leader Formulas says 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 consumers do if they have the recalled powder?
Stop using it and return it to the place of purchase for a full refund, according to the company. Consumers can contact Leader Formulas at Patrick@leaderformulas.com or 832-855-7562 during the hours listed in the recall notice.
Have any adverse events been reported?
Leader Formulas says it has not received reports of adverse events related to the recall. The announcement does not establish whether any unreported effects occurred. Consumers who experience a problem should contact a healthcare provider and may file a report with FDA MedWatch.
Source: primary
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