Night Bullet Capsules — Class I drug recall D-828-2013
Terminated recall by Green Planet Inc, reported 2013-08-07, distributed nationwide. Marketed Without an Approved NDA/ANDA; product contains analogues of sildenafil and tadalafil which are active
| Recall number | D-828-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Green Planet Inc, Riverside, CA, United States |
| Recall initiated | 2013-03-11 |
| Classified | 2013-07-29 |
| Reported by FDA | 2013-08-07 |
| Terminated | 2013-08-16 |
| Distributed | Nationwide (US) |
| Quantity | 429,619 capsules |
| Reason classes | unapproved product |
| Lot numbers | 10/15, B43N032 |
Product
Night Bullet Capsules, supplied in 1 count packets, produced by Green Planet Inc, Riverside, CA
Reason for recall
Marketed Without an Approved NDA/ANDA; product contains analogues of sildenafil and tadalafil which are active pharmaceutical ingredients in FDA-approved drugs used to treat erectile dysfunction (ED) making this product 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-828-2013. 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.