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FDA recall, , High risk

Rapture Pre Workout Berry Mojito, Electric Lemonade, and Rainbow Twist Dietary Supplement

Leader Formulas products contain DMAA.

Summary by Recall Canary from the FDA notice

What happened

FDA discovered presence of 1,3-dimethylamylamine (DMAA) in the product during product testing.

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.

More hidden drug ingredient recalls

2 photos

What to do

If a code on your package is listed below:

  1. Consumers who have purchased the RAPTURE Preworkout products which are being recalled should stop using the products.
  2. Return to the place of purchase for a full refund.
  3. Consumers with questions regarding this recall may contact Leader Formulas, LLC. by email at Patrick@leaderformulas.com or by phone at 832-855-7562 Monday through Friday 9 AM to 5 PM CT.
  4. Contact your physician or healthcare provider if you have experienced any problems that may be related to taking or using this drug product.

Is yours affected?

3 products

Match the UPC and lot code listed under your product.

A UPC is the number printed under a barcode.

  1. Rainbow Twist

    UPC
    • 710154236506
    Lot code
    • 260327-4

  2. Electric Lemonade

    UPC
    • 710143 236513
    Lot code
    • 260327-4

  3. Berry Mojito

    UPC
    • 710154236544
    Lot code
    • 260327-4

Recall details

Company began the recall
Sold in

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. 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).

Company
Leader Formulas
Hazard
Hidden drug ingredient
Risk

High risk

There is a reasonable chance that eating it could cause serious health problems or death.

FDA Class I recall · How risk is rated

Event ID
99852
Recall numbers
H-0004-2027 to H-0006-2027

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report

  3. Listed on Recall Canary

  4. In FDA's weekly enforcement report

  5. Classified by FDA

  6. Announced by the company

  7. Summary updated

Other hidden drug ingredient recalls

See all: Other hidden drug ingredient recalls

Summary by Recall Canary, written with AI · summary updated Oct 24, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)