FDA Drug recall D-828-2013
Night Bullet Capsules, supplied in 1 count packets, produced by Green Planet Inc, Riverside, CA
- FDA Drug
- Class I
- terminated
- Published 2013-08-07
On 2013-08-07 the FDA classified a Class I recall of Night Bullet Capsules, supplied in 1 count packets, produced by Green Planet Inc, Riverside, CA by Green Planet, citing 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 erect….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-828-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-03-11 |
| Published | 2013-08-07 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Green Planet |
| Distribution | US |
Product
Night Bullet Capsules, supplied in 1 count packets, produced by Green Planet Inc, Riverside, CA
Reason
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.
Identifiers
| code_info | Lot# B43N032, Exp 10/15 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-828-2013%22
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