# FDA recall F-2399-2014

> **Beta Labs** · Class I · food recall initiated 2013-06-20.

## Product

PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE  19711, UPC 670541599822

## Reason for recall

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

## Distribution

nationwide and UK

## Key facts

- **Recall number:** F-2399-2014
- **Recalling firm:** Beta Labs
- **Classification:** Class I
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2013-06-20
- **Report date:** 2014-09-03
- **Termination date:** 2014-12-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-2399-2014

## Citation

> AI Analytics. FDA recall F-2399-2014. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/F-2399-2014. Source: US FDA. Licensed CC0.

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