Mojo Nights — Class I drug recall D-327-2013
Terminated recall by Evol Nutrition, reported 2013-05-22, distributed nationwide. Marketed Without an Approved NDA/ANDA: The products were found to contain FDA approved ingredients and analogu
| Recall number | D-327-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Evol Nutrition, Kennesaw, GA, United States |
| Recall initiated | 2012-08-23 |
| Classified | 2013-05-16 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2013-07-22 |
| Distributed | Nationwide (US) |
| Quantity | 1,000 blister |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00718122119837 |
Product
Mojo Nights, 1 capsule, UPC 7 18122 11983 7, Distributed By: Mojo Health Lauderhill, FL 33351
Reason for recall
Marketed Without an Approved NDA/ANDA: The products were found to contain FDA approved ingredients and analogues of FDA approved ingredients used to treat male erectile dysfunction, making them unapproved new 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-327-2013. 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.