RAPTURE Pre-Workout Recall Details for Lot 260327-4
Consumers who use stimulant-heavy pre-workout powders should inspect their supplement shelves. Leader Formulas, LLC is conducting a voluntary nationwide recall of RAPTURE Preworkout lot 260327-4 after FDA laboratory testing confirmed undeclared 1,3-dimethylamylamine (DMAA), a stimulant that can raise blood pressure and cause serious cardiovascular problems. Although this recall covers one specific lot, a different lot number does not establish that the product is safe. The FDA had previously advised consumers not to purchase or use RAPTURE Preworkout after testing confirmed undeclared DMAA. This five-minute verification guide provides packaging criteria, toxicologist guidance, and return steps as of October 2026.
How to Check Whether Your RAPTURE Container Is Affected
The voluntary recall applies exclusively to 450-gram round plastic containers of RAPTURE Preworkout distributed nationwide across retail stores and internet sales channels between January 29, 2025, and May 25, 2026. Compare your product against the official parameters below to identify an affected tub:
Source: FDA recall notice and Leader Formulas' official recall announcement.
- Check the Stamp: Locate the printed manufacturing batch code on the bottom or side of the tub and verify if it reads 260327-4.
- Match the UPC Barcode: Compare the 12-digit UPC barcode on the product packaging with the three codes listed in the table above:
- Rainbow Twist: 710154236506
- Electric Lemonade: 710143236513
- Berry Mojito: 710154236544
- Inspect the Packaging: Confirm that the container is a 450-gram round plastic tub with red and black lettering and a rhinoceros-print seal on top.
- Quarantine the Item: If all identifiers match, stop using the powder and store the container away from other household members.
Why the FDA's Earlier Warning Matters More Than the Lot Code
This recall follows an earlier FDA safety warning about the same product:
- May 5, 2026 Alert: The FDA issued a formal public warning advising consumers not to purchase or use RAPTURE Preworkout after agency laboratory analysis confirmed the presence of undeclared DMAA.
- October 2026 Recall: The manufacturer posted a voluntary recall notice dated October 1, 2026, while the FDA recall database logged the company announcement on October 6, 2026, and published its notice on October 7, 2026.
The Scope Distinction
If your RAPTURE container displays a lot number other than 260327-4, do not treat that number as proof that the product is safe. The October recall specifically covers lot 260327-4, but the FDA May 5, 2026 advisory separately advised consumers not to purchase or use RAPTURE Preworkout. The narrower scope of the October recall does not confirm that other lots are clean.
Cardiovascular Risks and How DMAA Affects the Body
DMAA (1,3-dimethylamylamine) is an amphetamine derivative and central nervous system stimulant. The FDA states that DMAA does not meet the legal definition of a dietary ingredient. Dietary supplements containing DMAA are considered unlawful under federal law.
DMAA can narrow blood vessels and raise blood pressure, increasing cardiovascular stress. The FDA warns that DMAA can cause serious health problems, including shortness of breath, chest tightness, abnormal heart rhythms, and heart attack. The agency also warns that combining DMAA with other stimulant ingredients, such as caffeine, poses additional health risks.
Unlike the ordinary effects consumers may expect from a conventional pre-workout supplement, the presence of undeclared DMAA creates a separate safety concern. Symptoms alone cannot reliably determine whether someone has experienced DMAA toxicity, so consumers should not attempt to diagnose or rule out a serious reaction on their own.
Practical Action Steps If You Already Consumed RAPTURE
If you have consumed servings from an affected container, follow these practical steps to manage health concerns safely:
- Stop Consumption: Do not take additional scoops or share the tub with training partners. Retain the physical container for medical identification.
- Record Intake Data: Note the exact flavor, lot number, number of scoops taken, and whether energy drinks or caffeine were used at the same time.
- Contact Poison Help: If you have no symptoms but are concerned about possible exposure, or if you are unsure what to do, call 1-800-222-1222 or access the online tool at webPOISONCONTROL. Both services are free, confidential, and available 24 hours a day.
- Seek Emergency Care: Call 911 immediately if you experience chest tightness, radiating pain, severe shortness of breath, sustained palpitations, vision changes, or fainting.
Step-by-Step Return and Federal Reporting Instructions
Consumers who purchased RAPTURE Preworkout lot 260327-4 are instructed to return the product to their place of purchase for a full refund. Follow these return procedures:
- Return to the Retailer: Contact the store or online retailer where you purchased the product and ask how to return the recalled item for a full refund. If you purchased it directly from the manufacturer, contact Leader Formulas for instructions.
- Prepare Documentation: Gather your receipt, bank statement, or online order confirmation. Take photographs of the lot stamp and UPC before returning the item.
- Lost Receipt or Empty Container: The published recall notices do not specify whether purchases without receipts or empty containers qualify for a refund. Contact the original retailer first. If you need further instructions, contact Leader Formulas at 832-855-7562 or Patrick@leaderformulas.com, Monday through Friday, 9:00 a.m. to 5:00 p.m. Central Time.
- Report Adverse Events: If you experienced an unexpected reaction after using RAPTURE Preworkout, follow the FDA's current guidance for reporting problems with dietary supplements. Consumers can submit reports through the FDA Safety Reporting Portal. The FDA's product-specific RAPTURE safety notice also provides additional reporting instructions.
Recognizing Hidden Stimulant Names on Supplement Panels
While RAPTURE was cited for undeclared DMAA, unapproved stimulants in other products may appear under chemical synonyms or botanical labels. Watch for these ingredient names:
- Chemical Aliases: 1,3-DMAA, 1,3-dimethylamylamine, methylhexanamine, 2-amino-4-methylhexane, 4-methyl-2-hexanamine, or geranamine.
- Botanical Terms: Pelargonium graveolens extract or geranium extract. The FDA notes that these terms may indicate that DMAA is present, although the agency is not aware of reliable scientific evidence showing that DMAA occurs naturally in plants.
- Proprietary Blends: When individual ingredient amounts are not disclosed, it can be harder for consumers to evaluate the dose of each stimulant in the blend.
Independent Third-Party Certification Standards
In the United States, the FDA generally does not approve dietary supplements for safety and effectiveness before they are marketed. Manufacturers are responsible for ensuring their products comply with applicable laws, and the FDA can take enforcement action against products that violate those requirements.
Independent programs such as NSF Certified for Sport, Informed Choice, and BSCG offer different forms of supplement testing and quality verification. Depending on the program, these may include screening for prohibited substances, label review, or other quality checks. Testing scope and frequency vary by program and product. Certification can provide additional quality-control information, but it is not FDA approval and does not eliminate all health risks.
Frequently Asked Questions
Is RAPTURE Preworkout recalled nationwide?
Yes. Leader Formulas, LLC issued a nationwide voluntary recall for the affected lot. The product was distributed through brick-and-mortar retail outlets and online e-commerce platforms across the United States.
Which lot number and UPC barcodes are officially recalled?
The recall applies exclusively to lot number 260327-4. The three associated 12-digit UPC barcodes are Rainbow Twist (710154236506), Electric Lemonade (710143236513), and Berry Mojito (710154236544).
What if my RAPTURE container has a completely different lot number?
If your RAPTURE Preworkout has a lot number other than 260327-4, do not treat that number as proof that the product is safe. The October recall specifically covers lot 260327-4, but the FDA May 5, 2026 advisory separately advised consumers not to purchase or use RAPTURE Preworkout after laboratory testing found undeclared DMAA.
What should I do if I already took the supplement?
Stop taking the product immediately. If you have no symptoms but are concerned about possible exposure, or if you are unsure what to do, contact Poison Help at 1-800-222-1222 or visit webPOISONCONTROL for free, confidential guidance. If you experience severe symptoms like chest pressure, shortness of breath, irregular heartbeat, or fainting, call 911 or go to an emergency room immediately.
How can I request a refund if I lost my store receipt?
First, check your digital purchase records, email confirmations, or banking statements. Contact the original retailer first. If you need further instructions, contact Leader Formulas directly at 832-855-7562 or Patrick@leaderformulas.com for individual guidance.
How do I report a bad reaction from this supplement to the FDA?
Consumers can submit reports through the FDA Safety Reporting Portal following the agency guidance for dietary supplements. The FDA product-specific RAPTURE notice also provides additional reporting instructions.
What chemical names indicate DMAA on a supplement label?
DMAA can be listed under names such as 1,3-dimethylamylamine, 1,3-DMAA, methylhexanamine, 2-amino-4-methylhexane, or geranamine. Botanical listings like Pelargonium graveolens extract or geranium extract may also indicate its presence. The FDA states that DMAA is not a lawful dietary ingredient and that dietary supplements containing DMAA are illegal under federal law.
The Bottom Line
A verified lot number tells you whether a container falls under the October recall. It does not prove that a different production lot is safe.
Check your product's lot number and UPC to determine whether it matches the formal recall. However, the FDA's May 5, 2026, advisory warned consumers not to purchase or use RAPTURE Preworkout after testing confirmed undeclared DMAA. Do not assume that a different lot number establishes safety. Follow the FDA's current guidance and avoid using the product.
Sources and Medical References
Official Government and Manufacturer Records
- FDA: Leader Formulas, LLC Issues Voluntary Nationwide Recall of RAPTURE Preworkout
- FDA: Public Notification: RAPTURE Preworkout Contains Undeclared DMAA
- FDA: DMAA in Products Marketed as Dietary Supplements
- Leader Formulas: Official Product Recall Announcement
- Poison Control: National Hotline and Consultation Information
- webPOISONCONTROL: Online Exposure Assessment Tool
- FDA: How to Report a Problem with Dietary Supplements
- FDA: Safety Reporting Portal for Dietary Supplements
Independent Certification Standards
Comments
Post a Comment