CLASS II Drug recall · Reported 10 Apr 2013 · FDA Enforcement Report
Aniracetam and Choline, Aniracetam 460 mg recalled
Palmer Natural Products is recalling Aniracetam and Choline, Aniracetam 460 mg, Choline 76 mg per bottler, non-Rx, distributed in California, Florida, Idaho. The recall was initiated on 11 Mar 2013 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-232-2013
- FDA event ID
- 64619
- Recalling firm
- Palmer Natural Products, Star, ID
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 11 Mar 2013
- FDA classified
- 1 Apr 2013
- Reported
- 10 Apr 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Hidden Drug Ingredients
Timeline
| 11 Mar 2013 | Recall initiated by company | |
| 1 Apr 2013 | Classified by FDA | +21 days |
| 10 Apr 2013 | Published in enforcement report | +9 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 products are unapproved drugs
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 and Choline, Aniracetam 460 mg, Choline 76 mg, 180 capsules per bottler, non-Rx, distributed by BoostYourGrade, BoostYourGrade, LLC Orlando, FL
Where it was distributed
Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Questions about this recall
Is Aniracetam and Choline, Aniracetam 460 mg, Choline 76 mg per bottler, non-Rx recalled?
Yes. Palmer Natural Products recalled Aniracetam and Choline, Aniracetam 460 mg, Choline 76 mg per bottler, non-Rx on 11 Mar 2013. The recall is Class II and its status is Terminated. Recall number D-232-2013.
Why was it recalled?
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Which lots are affected?
All lot codes.
Where was it sold?
Florida, Idaho, California and Hong Kong. This product can be ordered on line.
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Palmer Natural Products
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Piracetam & Choline, 390mg Piracetam 104mg Choline Capsules, a), b) recalled | Palmer Natural Products | Hidden Drug Ingredients | CA, FL, ID |
| Drug | CLASS II | BoostYourGrade.com, Piracetam 390mg Choline 104mg capsules recalled | Palmer Natural Products | Hidden Drug Ingredients | CA, FL, ID |
| Drug | CLASS II | Nootropa Cognitive Enhancement Supplement recalled | Palmer Natural Products | Hidden Drug Ingredients | CA, FL, ID |
| Drug | CLASS II | Aniracetam & Choline capsules recalled by Palmer Natural Products | Palmer Natural Products | Hidden Drug Ingredients | CA, FL, ID |
| Drug | CLASS II | Oxiracetam & Choline , Oxiracetam 460mg Choline 110mg recalled | Palmer Natural Products | Hidden Drug Ingredients | CA, FL, ID |