Super Power capsules — Class I drug recall D-323-2013
Terminated recall by D& S Herbals, LLC, reported 2013-05-22, distributed nationwide. Marketed Without An Approved NDA/ANDA: This dietary supplement has been found to contain sildenafil, an FDA ap
| Recall number | D-323-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | D& S Herbals, LLC, Woodbridge, NJ, United States |
| Recall initiated | 2012-12-22 |
| Classified | 2013-05-16 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2013-08-12 |
| Distributed | Nationwide (US) |
| Quantity | 40,480 blister |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00718122906789 |
| Lot numbers | 06/15, L08108 |
Product
Super Power capsules, Proprietary Blend 570 mg, packaged in 2-count capsules per blister pack, Distributed by: Freedom Trading, NJ 08863, UPC 7 18122 90678 9.
Reason for recall
Marketed Without An Approved NDA/ANDA: This dietary supplement has been found to contain sildenafil, an FDA approved drug for the treatment of male erectile dysfunction making this an unapproved new drug.
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-323-2013. 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.