Drug recall
LIBIPOWER PLUS Capsules, Natural Male Stimulant, 650 mg herbal blend, packaged in 1 capsule blister packs…
FDA recall event 52653 · Class I · HALOTECO
Key facts
| Event ID | 52653 |
|---|---|
| Recall numbers | D-333-2010 |
| Recalling firm | HALOTECO |
| Product type | Drugs |
| Products | LIBIPOWER PLUS Capsules, Natural Male Stimulant, 650 mg herbal blend, packaged in 1 capsule blister packs, Manufactured for Haloteco, Los Angeles, CA |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Marketed without an approved NDA/ANDA: product found to contain tadalafil which is the active ingredient of an FDA approved drug for Erectile Dysfunction (ED). |
| Initiation date | Jun 25, 2009 |
| Termination date | Aug 1, 2012 |
| City | Santa Monica |
| State | CA |
| Country | United States |
| FEI number | 3007521738 |
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