RAPTURE Preworkout Pulled From Market After DMAA Found in Product

Recall Background

Leader Formulas, LLC. announced a voluntary recall of one lot of RAPTURE Preworkout dietary supplement powder after FDA testing detected 1,3-Dimethylamylamine, or DMAA, in the product. The company said the recall was made with the knowledge of the U.S. Food and Drug Administration and was later published. The supplement was sold nationwide at retail and through the company website. Leader Formulas, LLC. said it is contacting distributors and customers by mail and arranging for the return of recalled products. No adverse events had been reported at the time of the notice.

Why the Product Was Recalled

The recall was issued because the supplement was found to contain DMAA. According to the notice, use of DMAA may raise blood pressure and can create cardiovascular risks, including heart attack, shortness of breath, and chest tightness.

Recalled Product Details

The recalled item is RAPTURE Preworkout dietary supplement powder in 450g round plastic containers with red and black lettering and a rhinoceros print seal on the top.

The flavors listed in the notice are:

• Rainbow Twist
• Electric Lemonade
• Berry Mojito

The recall covers one lot: 260327-4.

How to Spot the Recalled Items

Consumers are advised to check the product UPC and lot number.

UPC/product identifiers listed in the notice are:

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

Lot number: 260327-4

Packaging: 450g round plastic containers with red and black lettering and a rhinoceros print seal on top of the container.

The notice also includes product images showing the recalled packaging.

For more information about the recall, visit the FDA notice: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/leader-formulas-llc-issues-voluntary-nationwide-recall-rapture-preworkout-due-presence-13