MODERATE RISK Terminated F-2400-2014

PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802

Recalled by Beta Labs

Classification

Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.

The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.

Product Quantity

743 units

Product Type

Food

Code Info

Lot # 1205129, Exp 12/16

Voluntary/Mandated

Voluntary: Firm initiated

Distribution Pattern

nationwide and UK

Company Location

Memphis, TN, 38103-6429

Report Date

09/03/2014

Recall Initiated

06/20/2013

Classification Date

08/27/2014

Termination Date

12/03/2014

Source: U.S. Food & Drug Administration (FDA) — FDA Recalls

Last updated: August 30, 2026

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