A B Aniracetam Fast Acting Nootropic Dietary Supplement Recall

Why it was recalled

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

Product description

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

Lot numbers, UPCs & expiration codes

Lot # 32000311

Where it was sold

In retail store located in TX and internet sales nationwide.

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-196-2013
Classification: Class II
Status: Terminated
Recall initiated: May 27, 2011
FDA report date: Mar 20, 2013
Quantity: 912 bottles
Recall type: Voluntary: Firm initiated
Recalling firm: A B Nutrition, Inc.

Original FDA data

Every field from FDA enforcement report D-196-2013, exactly as published.

Show all FDA fields

City: Spring
State: TX
Status: Terminated
Country: United States
Event ID: 59001
Address: 5407 Louetta, Suite E
Code information: Lot # 32000311
Postal code: 77379
Report date: Mar 20, 2013
Product type: Drugs
Recall number: D-196-2013
Classification: Class II
Recalling firm: A B Nutrition, Inc.
Product quantity: 912 bottles
Termination date: Jul 29, 2013
Reason for recall: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Voluntary / mandated: Voluntary: Firm initiated
Product description: ANIRACETAM FAST ACTING NOOTROPIC Dietary Supplement PHARMACEUTICAL GRADE 750mg 60 Capsules per bottle CTD Labs Houston, TX 77090
Distribution pattern: In retail store located in TX and internet sales nationwide.
Recall initiation date: May 27, 2011
Initial firm notification: E-Mail
Center classification date: Mar 8, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-196-2013, published Mar 20, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

ANIRACETAM FAST ACTING NOOTROPIC Dietary Recall

Summary