CLASS II Drug recall · Reported 10 Apr 2013 · FDA Enforcement Report

Brain Defogger, Piracetam 390mg Choline 104mg capsules recalled

Palmer Natural Products is recalling Brain Defogger, Piracetam 390mg Choline 104mg capsules, 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

Lot, batch or date codesAll lot codes.
Quantity recalled4103 bottles

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-234-2013
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

Timeline

11 Mar 2013Recall initiated by company
1 Apr 2013Classified by FDA+21 days
10 Apr 2013Published 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

Brain Defogger, Piracetam 390mg Choline 104mg capsules, 100 count bottle, OTC, BoostYourGrade, LLC, Orlando, FL. .

Where it was distributed

Florida, Idaho, California and Hong Kong. This product can be ordered on line.

CaliforniaFloridaIdaho

Questions about this recall

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 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

6 other products · FDA event 64619

This product is part of a recall event; the main page for the event is Aniracetam and Choline, Aniracetam 460 mg recalled.

More recalls from Palmer Natural Products

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