Oxiracetam & Choline — Class II drug recall D-236-2013
Terminated recall by Palmer Natural Products, reported 2013-04-10, distributed in CA, FL, ID. Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
| Recall number | D-236-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Palmer Natural Products, Star, ID, United States |
| Recall initiated | 2013-03-11 |
| Classified | 2013-04-01 |
| Reported by FDA | 2013-04-10 |
| Terminated | 2013-08-07 |
| Distributed | CA, FL, ID |
| Countries outside the US | HK |
| Reason classes | unapproved product |
Product
Oxiracetam & Choline , Oxiracetam 460mg Choline 110mg capsules a) 30 count bottle, b) 60 count bottle, c) 90 count bottle, OTC, BoostYourGrade, LLC, Orlando, FL. 32826
Reason for recall
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-236-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.