Leader Formulas Recalled RAPTURE Preworkout Supplement

Consumers nationwide are advised to check their supplement lot numbers due to a restricted ingredient discovery.

Updated on Oct. 7, 2026 in Body Building

Rows of generic, textless supplement bottles arranged on shelves in a bright, modern retail store aisle.
Leader Formulas, LLC. has issued a voluntary recall for 450g containers of RAPTURE Preworkout following an FDA discovery of an unapproved stimulant. AI Illustration. Upload story photo >

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Leader Formulas, LLC. has issued a voluntary recall for 450g containers of RAPTURE Preworkout. The recall follows an FDA discovery that the product contains 1,3-Dimethylamylamine (DMAA), an ingredient that prompted this national action.

Why it matters

The presence of DMAA in supplements is a health concern due to its potential impact on cardiovascular systems and blood pressure. This recall ensures that products containing the unapproved substance are removed from the market to prevent consumer exposure.

FDA testing confirmed the presence of 1,3-Dimethylamylamine in lot number 260327-4 of the product. While no adverse events have been reported to date, the recall covers all units distributed nationwide between 1/29/25 and 5/25/26.

The players

Leader Formulas, LLC.

A Tomball, TX-based company that manufactures and distributes nutritional supplements and exercise products.

FDA

The federal agency responsible for protecting public health by regulating the safety of dietary supplements and food products.

The details

DMAA, or 1,3-Dimethylamylamine, is a stimulant previously associated with negative cardiovascular effects including increased blood pressure and heart rate. The FDA identifies DMAA as a substance that should not be present in dietary supplements, leading to the voluntary recall of all 450g containers from the affected lot. The company is actively contacting distributors and customers to facilitate returns and refunds for the identified lot.

Timeline

  1. The product was distributed nationwide from 1/29/25 to 5/25/26.

  2. The official recall notification was issued on 10/7/26.

Health Landscape

The removal of products containing DMAA follows a long-standing regulatory pattern by the FDA to ensure supplement safety. This action reinforces the agency's authority under the Dietary Supplement Health and Education Act to pull products that do not meet established safety criteria.

If you have 450g containers of RAPTURE Preworkout, check the bottom for lot number 260327-4 and return it to your place of purchase for a refund. If you have concerns about your health after using this product, schedule a conversation with your physician.

The takeaway

Supplements that contain unapproved stimulants like DMAA present health risks that require immediate market removal. When a recall occurs, always stop use of the specific lot number and consult a healthcare professional regarding any unexplained symptoms or health history concerns.

Further reading

For more on supplement safety and ingredient standards, visit the Body Building section.

More information

To report adverse reactions or learn about safety alerts, visit the FDA MedWatch Adverse Event Reporting program.

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Do you generally trust that dietary supplements sold in stores are safe for consumer use?