Why it was recalled
The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
Product description
PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599822
Lot numbers, UPCs & expiration codes
Lot # 58800512, Exp 05/16
Where it was sold
nationwide and UK
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-2399-2014
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Jun 20, 2013
- FDA report date
- Sep 3, 2014
- Quantity
- 2154 units
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Beta Labs
Original FDA data
Every field from FDA enforcement report F-2399-2014, exactly as published.
Show all FDA fields
- City
- Memphis
- State
- TN
- Status
- Terminated
- Country
- United States
- Event ID
- 65585
- Address
- 2 W GE Patterson Ave Apt 103
- Code information
- Lot # 58800512, Exp 05/16
- Postal code
- 38103-6429
- Report date
- Sep 3, 2014
- Product type
- Food
- Recall number
- F-2399-2014
- Classification
- Class I
- Recalling firm
- Beta Labs
- Product quantity
- 2154 units
- Termination date
- Dec 3, 2014
- Reason for recall
- The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599822
- Distribution pattern
- nationwide and UK
- Recall initiation date
- Jun 20, 2013
- Initial firm notification
- Press Release
- Center classification date
- Aug 27, 2014