F-2400-2014 Class II Terminated
FDA food recall F-2400-2014 was initiated by Beta Labs on June 20, 2013 and is designated Class II. 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: 743 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
- 743 units
Product Description
PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802
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 # 1205129, Exp 12/16