Beta Labs: Food Recall in 2014 - (Recall #: F-2400-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802

Product Classification:

Class II

Date Initiated: June 20, 2013

Date Posted: September 3, 2014

Recall Number: F-2400-2014

Event ID: 65585

Reason for Recall:

The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.

Status: Terminated

Product Quantity: 743 units

Code Information:

Lot # 1205129, Exp 12/16

Distribution Pattern:

nationwide and UK

Voluntary or Mandated:

Voluntary: Firm initiated