Is Arom-X Capsules Dietary Supplement, Anti-Estrogen Complex (3a-Hydroxyetioallocholan Ethyl Ester 30mg, 1,4,6 etioallocholan-dione 5mg), sold in 60 count bottles (UPC 893461001002) and 80 count bottles (UPC 893461001033), sold individually and in promotional "Kits", Natural Testosterone Booster, Libido Enhancer, Manufactured for Advanced Muscle Science, Las Vegas, NV recalled?

Critical RiskFDA Drug

Dcd Llc: Marketed without an Approved NDA/ANDA; product contains 1,4,6 etioallocholan-dione as an ingredient on the label, which is a synonym for the same ingredient, commonly known as ATD. ATD is an aromatase inhibitor which is not a dietary ingredient; Marketed without an Approved NDA/ANDA; product contains 3,17-keto-etiochol-triene as an ingredient on the label, which is a synonym for the same ingredient, commonly known as ATD. ATD is an aromatase inhibitor which is not a dietary ingredi

Agency Publication Date: January 18, 2011

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 56990

Status: Resolved

Manufacturer: Dcd Llc

Manufactured In: United States

Units Affected: 5 products (Per firms distribution records, approximately 9,208 bottles of the Arom-X (60) and (80) capsules were distributed between 4/1/2009 to 9/16/2010.; Per firms distribution records, approximately 8,501 bottles of the Arom-X UTT (60mL) liquid were distributed between 4/1/2009 to 9/16/2010.; Per firms distribution records, approximately 4,518 bottles of the Arom-XL (120mL) and (100) capsules were distributed between 4/1/2009 to 9/16/2010; Per firms distribution records, approximately 1,389 bottles of the 4-AD (60) capsules were distributed between 4/1/2009 to 9/16/2010.; Per firms distribution records, approximately 7,867 bottles of the Decavol (63) capsules were distributed between 4/1/2009 to 9/16/2010.)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

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