Home / Recalls / Beta Labs / F-2400-2014

F-2400-2014 Class II Terminated

Recalled by Beta Labs — Memphis, TN

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

Other recalls by Beta Labs

  • F-2401-2014 Class II — RED VIPERS, ADVANCED FOCUS AND CONCENTRATION, HEIGHTENED ENERGY LEVELS, 75mg EPH (June 20, 2013)
  • F-2398-2014 Class II — Oxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEAS (June 20, 2013)
  • F-2399-2014 Class I — PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULE (June 20, 2013)