RAPTURE Preworkout Recall 2026: Lot, UPCs and Refund

Quick answer: Leader Formulas LLC has voluntarily recalled one lot of RAPTURE Preworkout because the product contains 1,3-dimethylamylamine (DMAA), an ingredient the U.S. Food and Drug Administration says can raise blood pressure and may lead to serious cardiovascular problems. The affected lot is 260327-4. Consumers should stop using the recalled product and return it for a full refund.

The FDA published the recall notice on October 7, 2026. The recall covers 450-gram round containers sold nationwide through retail stores and online between January 29, 2025 and May 25, 2026. The FDA notice says no adverse events had been reported to Leader Formulas at the time of the announcement.

Which RAPTURE Preworkout products are recalled?

The recall applies to a single production lot, but it covers three flavors with different UPCs. Check both the flavor and the lot number printed on the container before deciding whether your product is affected.

If your container has a different lot number, the FDA notice does not identify it as part of this recall. If the lot number is unreadable or missing, contact the manufacturer rather than guessing.

Why is RAPTURE Preworkout being recalled?

The stated reason is the presence of DMAA. The FDA has long warned that DMAA can narrow blood vessels and arteries, which can increase blood pressure and place additional stress on the cardiovascular system. The agency says the ingredient may be associated with serious effects including shortness of breath, tightening in the chest and heart attack.

This recall is not based on a packaging typo or a minor labeling issue. It concerns an ingredient with a potential health risk, which is why consumers should follow the stop-use instructions rather than continue using the product while waiting for more information.

What should you do if you have a recalled container?

1. Stop using the product immediately.
2. Check the flavor, UPC and lot number against the table above.
3. Keep the container and proof of purchase if available.
4. Return the recalled product to the place of purchase for a full refund, following the recall instructions.
5. If you experienced a health problem after using the product, contact a medical professional and consider reporting the event through the FDA’s MedWatch system.

The official recall notice is available on the FDA website. AVARIXO will update this guide if the FDA expands the recall or the company publishes additional affected lots.

How to identify the recalled product

The recalled product is sold in 450-gram round containers under the RAPTURE Preworkout name. Because the recall spans three flavors, the flavor name alone is not enough to identify an affected unit. The most reliable check is the lot number 260327-4, followed by the UPC for the flavor you purchased.

Consumers who bought the product online should also check old order confirmations. Those records can help establish the purchase date and retailer if the label is difficult to read.

Are any illnesses or injuries reported?

According to the FDA recall notice, Leader Formulas had not received reports of adverse events connected with the recalled product when the notice was published. That does not change the recall advice: consumers are still instructed to stop using the affected lot.

Why this recall matters for supplement buyers

Preworkout products can contain multiple stimulants, and ingredient names are not always familiar to shoppers. A recall involving DMAA is a reminder to check both the label and current safety alerts, especially for products purchased months earlier and stored for later use.

For other active consumer safety notices, see AVARIXO’s Alerts section, the Avarixo Product Recall Tracker, and our recent HotHands rechargeable hand warmer recall guide.

FAQ

What RAPTURE Preworkout lot is recalled?

Lot 260327-4 is the lot identified in the FDA notice.

Which flavors are included?

Rainbow Twist, Electric Lemonade and Berry Mojito are listed, each with a separate UPC.

What is the reason for the recall?

The product contains DMAA, which the FDA says can raise blood pressure and create potentially serious cardiovascular risks.

Can I get a refund?

Yes. The recall notice instructs consumers to return affected product for a full refund.

Were injuries reported?

No adverse events had been reported to the company when the FDA published the recall notice on October 7, 2026.