F-2399-2014 Class I Terminated
FDA food recall F-2399-2014 was initiated by Beta Labs on June 20, 2013 and is designated Class I. Reason for recall: The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements. The recall status is terminated (terminated December 3, 2014). Affected quantity: 2154 units.
Recall Details
- Product Type
- Food
- Report Date
- September 3, 2014
- Initiation Date
- June 20, 2013
- Termination Date
- December 3, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2154 units
Product Description
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 Pattern
nationwide and UK
Code Information
Lot # 58800512, Exp 05/16