Elevated risk U.S. Food and Drug Administration

Rapture Preworkout Dietary Supplement Powder recall: Product contains 1,3-Dimethylamylamine (DMAA)

Recall published 22 days ago

Product contains 1,3-Dimethylamylamine (DMAA)

Rapture Dietary supplements — recalled dietary supplementsRapture Dietary supplements — recalled dietary supplements (photo 2)Rapture Dietary supplements — recalled dietary supplements (photo 3)
3 photos published by U.S. Food and Drug Administration with the recall notice.

The hazard: Drug safety concern

A problem with this medicine prompted the recall. With prescriptions, the first move is a conversation rather than a decision.

What the notice says: Using DMAA can result in elevated blood pressure and could lead to cardiovascular problems, including heart attack, shortness of breath and tightening of the chest.

Why it matters: The FDA recorded an enforcement action against this product. The classification and the summary above describe how serious the agency considers it.

Recall details

Published
October 6, 2026
Risk level
Elevated risk
Issued by
U.S. Food and Drug Administration
Brand
Rapture
Product type
Dietary supplements
Distribution
Nationwide
UPC codes
710154236506, 710143236513, 710154236544

Products covered by this recall

Preworkout Dietary Supplement Powder

What the company announced

Leader Formulas, LLC. of Tomball, TX, is voluntarily recalling one (1) lot of RAPTURE Pre workout, a dietary supplement powder because it was found to contain 1,3-Dimethylamylamine (DMAA) and sold at the consumer level. Using DMAA can result in elevated blood pressure and could lead to cardiovascular problems, including heart attack, shortness of breath and tightening of the chest.

The product is used as a dietary supplement and is packaged in 450g round plastic containers with red and black lettering and a rhinoceros print seal on top of the container. The affected RAPTURE Preworkout lots include the following lot number (260327-4). The product can be identified by the following:

  • PRODUCT: Rainbow Twist · UPC: 710154236506
  • PRODUCT: Electric Lemonade · UPC: 710143 236513
  • PRODUCT: Berry Mojito · UPC: 710154236544

RAPTURE Preworkout was distributed between 1/29/25 to 5/25/26 Nationwide to retail and via internet through the company website ( www.leaderformulas.com ).

The issue was discovered in the product during testing by the FDA. Leader Formulas, LLC. is notifying its distributors and customers by mail and is arranging for return of all recalled products. Consumers who have purchased the RAPTURE Preworkout products which are being recalled should stop using the products and return to the place of purchase for a full refund.

Leader Formulas, LLC. has not received any reports of adverse events related to this recall.

Consumers with questions regarding this recall may contact Leader Formulas, LLC. by email at [email protected] or by phone at 832-855-7562 Monday through Friday 9 AM to 5 PM CT.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Online : Complete and submit the report: www.fda.gov/medwatch/report.htm

Regular Mail or Fax : Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-3321088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Reproduced from the company announcement posted on fda.gov. Links and contact forms in the original are not repeated here; the official notice below has them.

Check your product

The notice names 5 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 710154236506
  • 710143236513
  • 710154236544

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • of RAPTURE Pre workout

Model or item number

On the rating label, the box or the instruction sheet.

  • LLC

Codes are lifted verbatim from the FDA — Company recall announcements notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Drug safety

Rapture — A problem with this medicine prompted the recall. With prescriptions, the first move is a conversation rather than a decision.

  1. Check the lot number on your pack against the codes listed above.
  2. Ask the dispensing pharmacy for a replacement from an unaffected lot.
  3. Keep the carton; the lot number is often printed only on the outer pack.
  4. Report side effects you think the product caused to FDA MedWatch.

Getting a replacement supply

Do not let a refund question interrupt your treatment. Deal with the supply first and the money second.

  • Call the pharmacy before you run low. They can see which lot they dispensed to you and will usually swap it the same day.
  • Insurers do not normally count a recall replacement against a refill limit. If one is refused, ask the pharmacist to call it through as a recall override.
  • Over-the-counter products are refunded at the till like any other purchase; the recall notice on your phone is enough to explain the return.
  • If the manufacturer runs a direct reimbursement form, it will be linked from the official notice on this page.

Remedy named in the notice: Consumers who have purchased the RAPTURE Preworkout products which are being recalled should stop using the products and return to the place of purchase for a full refund.

Company contact: Leader Formulas, LLC. — Consumers: Leader Formulas, LLC., 832-855-7562, [email protected]

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Company recall announcements record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Rapture dietary supplements recalled?

Product contains 1,3-Dimethylamylamine (DMAA) Using DMAA can result in elevated blood pressure and could lead to cardiovascular problems, including heart attack, shortness of breath and tightening of the chest.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 710154236506, 710143236513, 710154236544; lot code of RAPTURE Pre workout; model number LLC. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Check the lot number on your pack against the codes listed above.

Can I get my money back?

The notice says: Consumers who have purchased the RAPTURE Preworkout products which are being recalled should stop using the products and return to the place of purchase for a full refund.

Where was the recalled product sold?

It was distributed nationwide.

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