FDAFDA · Food and drugs·Recall number F-2400-2014
PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802
Published September 3, 2014 · Recall initiated: June 20, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Beta Labs
- Distributor
- nationwide and UK
- Lot
- Lot # 1205129, Exp 12/16
- Risk classification
- Class II
- Area (FDA)
- food
- Country
- United States
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