Leader Formulas, LLC. Issues Voluntary Nationwide Recall of RAPTURE Preworkout Due to the Presence of 1,3-Dimethylamylamine (DMAA)
Official notice
7 Oct 2026
Last checked
13 Oct 2026
An official FDA notice concerns Rainbow Twist. The notice reports a serious safety risk. Stop using the product and follow the official notice. Published 2026-10-07.
What to do now
Instructions for consumers are available in the official FDA notice.
Official notice
2026-10-07
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Affected products
Product 1
Product 2
Product 3
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Rapture. Contact: Leader Formulas, LLC.. Phone 832-855-7562, 1-800-3321088.
Source & status
Source & status
Recall details
Recall details
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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