Man King Capsules — Class I drug recall D-1699-2012
Terminated recall by www.vitaminbestbuy.com, reported 2012-10-03, distributed nationwide. Marketed Without an Approved ANDA/NDA: presence of sildenafil.
| Recall number | D-1699-2012 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | www.vitaminbestbuy.com, Brewerton, NY, United States |
| Recall initiated | 2012-02-23 |
| Classified | 2012-09-26 |
| Reported by FDA | 2012-10-03 |
| Terminated | 2018-11-01 |
| Distributed | Nationwide (US) |
| Quantity | 69 boxes |
| Reason classes | unapproved product |
Product
Man King Capsules, 2800 mg, boxes of 5 packets, OTC, Developed by: American Wanbao Pharmaceutical International Group and Hainan Wanbao Biological Engineering Co., Ltd., 27 Heping Road, Haikou, Henan Province, UPC 9 009900 0032328
Reason for recall
Marketed Without an Approved ANDA/NDA: presence of sildenafil.
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-1699-2012. 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.