# FDA recall D-232-2013

> **Palmer Natural Products** · Class II · drug recall initiated 2013-03-11.

## Product

Aniracetam and Choline, Aniracetam 460 mg, Choline 76 mg, 180 capsules per bottler, non-Rx, distributed by BoostYourGrade, BoostYourGrade, LLC  Orlando, FL

## Reason for recall

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

## Distribution

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

## Key facts

- **Recall number:** D-232-2013
- **Recalling firm:** Palmer Natural Products
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-03-11
- **Report date:** 2013-04-10
- **Termination date:** 2013-08-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Star, ID, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-232-2013

## Citation

> AI Analytics. FDA recall D-232-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-232-2013. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
