FDA recall F-2400-2014

Beta Labs · Class II · food

Product

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

nationwide and UK

Key facts

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

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-2400-2014