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Beta Labs
FDA recall F-2400-2014 · Class II · reported 2014-09-03 · Terminated
- Product
- PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802
- Reason
- The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
- Quantity
- 743 units
- Distribution
- nationwide and UK
- Firm location
- TN, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Press Release
- Recall started
- 2013-06-20
- Terminated
- 2014-12-03
- Code info
- Lot # 1205129, Exp 12/16
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.