CLASS II Drug recall · Reported 20 Mar 2013 · FDA Enforcement Report
Aniracetam Fast Acting Nootropic Dietary Supplement recalled
A B Nutrition is recalling Aniracetam Fast Acting Nootropic Dietary Supplement Pharmaceutical Grade 750mg per bottle, distributed nationwide in the US. The recall was initiated on 27 May 2011 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-196-2013
- FDA event ID
- 59001
- Recalling firm
- A B Nutrition, Spring, TX
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 27 May 2011
- FDA classified
- 8 Mar 2013
- Reported
- 20 Mar 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Hidden Drug Ingredients
Timeline
| 27 May 2011 | Recall initiated by company | |
| 8 Mar 2013 | Classified by FDA | +651 days |
| 20 Mar 2013 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
ANIRACETAM FAST ACTING NOOTROPIC Dietary Supplement PHARMACEUTICAL GRADE 750mg 60 Capsules per bottle CTD Labs Houston, TX 77090
Where it was distributed
In retail store located in TX and internet sales nationwide.
Questions about this recall
Why was it recalled?
Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Which lots are affected?
Lot # 32000311
Where was it sold?
In retail store located in TX and internet sales nationwide.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
2 other products · FDA event 59001This product is part of a recall event; the main page for the event is Piracetam Cognition Enhancing Agent Dietary Supplement recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Piracetam Cognition Enhancing Agent Dietary Supplement recalled | A B Nutrition | Hidden Drug Ingredients | Nationwide | |
| CLASS II | Piracetam Powder Cognition Enhancing Agent Dietary recalled | A B Nutrition | Hidden Drug Ingredients | Nationwide |
More recalls from A B Nutrition
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Piracetam Powder Cognition Enhancing Agent Dietary recalled | A B Nutrition | Hidden Drug Ingredients | Nationwide |
| Drug | CLASS II | Piracetam Cognition Enhancing Agent Dietary Supplement recalled | A B Nutrition | Hidden Drug Ingredients | Nationwide |