Product Wiki · Recalls · U.S. FDA — Food Enforcement

Recall F-2400-2014 — PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802

U.S. FDA — Food Enforcement · United States · 2013-06-20 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Food Enforcement
Recall identifier
F-2400-2014
Date of alert
2013-06-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Beta Labs
Product category
food
Product type
Food
Barcode (EAN/GTIN)
029882559802
Reported risk: The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.