Hard Ten Days Capsule — Class I drug recall D-1698-2012
Terminated recall by www.vitaminbestbuy.com, reported 2012-10-03, distributed nationwide. Marketed Without an Approved ANDA/NDA: presence of sildenafil
| Recall number | D-1698-2012 |
|---|---|
| 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 | 550 boxes |
| Reason classes | unapproved product |
Product
Hard Ten Days Capsule, 4500 mg, boxes of 6 packets, OTC, Developed by: American Federal International Living Creature Group and Tibet Gold Source Living Creature Engineering Limited Company, Unit 18, 55 Beijing Road Central, Lhasa, Tibet
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-1698-2012. 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.