ANNOUNCED ONGOING Food recall · Reported 7 Oct 2026 · FDA company announcement, classification pending
Rapture Preworkout Dietary Supplement Powder recalled by Leader Formulas
Leader Formulas is recalling Rapture Preworkout Dietary Supplement Powder, distributed nationwide in the US. The recall was initiated on 6 Oct 2026 and is listed as ongoing.
Recall details
- Recall number
- FDA-PR-fd9a7808088c
- Recalling firm
- Leader Formulas
- Brand
- RAPTURE
- Classification
- Pending
- Status
- Ongoing
- Recall initiated
- 6 Oct 2026
- Reported
- 7 Oct 2026
- Reason category
- Hidden Drug Ingredients
- Product category
- Energy Drinks
Timeline
| 6 Oct 2026 | Recall initiated by company | |
| 7 Oct 2026 | Published in enforcement report | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product contains 1,3-Dimethylamylamine (DMAA). 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 UPC Rainbow Twist 710154236506 Electric Lemonade 710143 236513 Berry Mojito 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 Patric
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the company
RAPTURE Preworkout Dietary Supplement Powder
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Product contains 1,3-Dimethylamylamine (DMAA). 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 UPC Rainbow Twist 710154236506 Electric Lemonade 710143 236513 Berry Mojito 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 Patric
Where was it sold?
Nationwide
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does an unclassified recall mean?
The FDA assigns a class once it has assessed the health risk. Until then the recall is listed without one.
Read the official FDA notice · Source record retrieved 7 Oct 2026. This is a company announcement published by the FDA; the FDA has not yet classified the recall. The record is updated when the classification appears in the Enforcement Report. This page reports the record and gives no medical advice.
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