Unapproved Aniracetam and Choline Capsules Recalled by FDA
Palmer Natural Products is recalling Aniracetam & Choline capsules because they were marketed without an approved NDA or ANDA.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity level for unapproved drugs where no specific injuries or illnesses are reported in the source text.
Plain-English summary
Palmer Natural Products is recalling Aniracetam & Choline capsules, 430mg Aniracetam 88mg Choline, in 30, 60, 90, and 180 count bottles. The recall is being conducted because the products are unapproved drugs that were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
The affected products were distributed in Florida, Idaho, California, and Hong Kong, and can also be ordered online. The recall includes all lot codes for the 30, 60, 90, and 180 count bottle sizes.
Consumers who have purchased these products should stop using them and contact the recalling firm for further instructions.
The recalled product
- Product
- Aniracetam & Choline capsules, 430mg Aniracetam 88mg Choline, a) 30 count bottle b) 60 count bottle, c) 90 count, d) 180 count , OTC, BoostYourGrade, LLC Orlando, FL 32826
- Manufacturer
- Palmer Natural Products
- Category
- Drug — Unapproved Drug
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All lot codes.
Distribution
Part of a larger recall action
This product is one of 7 recalled by Palmer Natural Products under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 7 products in this recall →Related recalls
Same manufacturer · Palmer Natural Products
See all →- SevereFDA Recalls Unapproved Nootropa Cognitive Enhancement Supplement
FDA (Drugs) · 2013-04-10
- ModerateFDA Recalls Unapproved Piracetam and Choline Capsules Sold Online
FDA (Drugs) · 2013-04-10
- ModerateUnapproved Aniracetam and Choline Capsules Recalled by FDA
FDA (Drugs) · 2013-04-10
- ModeratePalmer Natural Products Recalls Unapproved Oxiracetam and Choline Capsules
FDA (Drugs) · 2013-04-10
- ModerateFDA Recalls Unapproved Brain Defogger Capsules Sold Online
FDA (Drugs) · 2013-04-10
Same hazard · unapproved drug
See all →- CriticalBuy-Herbal Recalls Kian Pee Wan Capsules for Undeclared Drug Ingredients
FDA (Drugs) · 2026-08-19
- SevereMR. 7 Super capsules recalled as Class I over undeclared sildenafil
FDA (Drugs) · 2026-03-11
- SevereMojo Max Fusion capsules recalled as Class I over undeclared drug ingredients
FDA (Drugs) · 2026-03-11
- SevereSilintan herbal pills recalled as Class I for undeclared meloxicam
FDA (Drugs) · 2026-03-11
- SevereAgebox iKids-Growth Day Formula Capsules Recalled Over Undeclared Drug Ingredient
FDA (Drugs) · 2026-03-04