US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 27, 2011 (15 years ago)

ANIRACETAM FAST ACTING NOOTROPIC Dietary Supplement PHARMACEUTICAL GRADE 750mg 60…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.

What was recalled

ANIRACETAM FAST ACTING NOOTROPIC Dietary Supplement PHARMACEUTICAL GRADE 750mg 60 Capsules per bottle CTD Labs Houston, TX 77090

Recalling firm
A B Nutrition, Inc.
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-196-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.