Drug recall
NASUTRA Herbal Supplement for Men, proprietary blend of ten chinese herbs, 300mg, packaged in blisters of 2…
FDA recall event 36159 · Class I · Nasutra LLC
Key facts
| Event ID | 36159 |
|---|---|
| Recall numbers | D-438-2007 |
| Recalling firm | Nasutra LLC |
| Product type | Drugs |
| Products | NASUTRA Herbal Supplement for Men, proprietary blend of ten chinese herbs, 300mg, packaged in blisters of 2 capsules, Distributed by Nasutra LLC, Beverly Hills, CA |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Unapproved New Drug; Product contains undeclared acetildenafil, an analogue of sildenafil |
| Initiation date | Sep 5, 2006 |
| Termination date | Aug 7, 2012 |
| City | Beverly Hills |
| State | CA |
| Country | United States |
| FEI number | 3005314987 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports