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Class II FDA

Leader Formulas Rapture Preworkout recalled over Undeclared allergen

Status: Ongoing · Recalled October 6, 2026 · Updated October 7, 2026
Leader Formulas Rapture Preworkout was recalled on October 6, 2026 because of undeclared allergen. It is a Class II recall (possible temporary or reversible harm). Affected area: nationwide. Do not eat this product. Return it to the place of purchase for a full refund.
HazardUndeclared allergen
Risk levelClass II
Affected areaNationwide
CategoryFood

What to do

Do not eat this product. Return it to the place of purchase for a full refund.

Confirm the details against the official FDA notice before acting.

Does this affect you?

Check the product in your home against the recalled item:

Product as filed
Leader Formulas, LLC. — Voluntary Nationwide Recall of RAPTURE Preworkout Due to the Presence of 1,3-Dimethylamylamine (DMAA)
Sold at
leaderformulas.com

Full recall details

Reason for recall
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 cardiovascula
Hazard class
Class II — possible temporary or reversible harm
Recalling company
Leader Formulas, LLC.
Recall type
Voluntary
Quantity
Distribution
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).

Frequently asked questions

Is Leader Formulas Rapture Preworkout recalled?

Yes. It was recalled on October 6, 2026 because 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 cardiovascula.

What should I do if I have it?

Do not eat this product. Return it to the place of purchase for a full refund.

Which states are affected?

This recall is nationwide.

How do I identify the recalled product?

The notice lists no UPC or lot code. Match the brand, product name and package size against the official FDA notice.

How serious is a Class II recall?

Class II means possible temporary or reversible harm.

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