Drug recall
Sanapac''s Vee 200 for Men. The product is sold in 90 cc and 120 cc bottles of 30 and 50 tablets. The product…
FDA recall event 30883 · Class II · Sanapac Co
Key facts
| Event ID | 30883 |
|---|---|
| Recall numbers | F-185-5 |
| Recalling firm | Sanapac Co |
| Product type | Food |
| Products | Sanapac''s Vee 200 for Men. The product is sold in 90 cc and 120 cc bottles of 30 and 50 tablets. The product is shipped in cases containing 12 bottles. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The product is adulterated since it contains the new dietary ingredient, androstenedione, for which there is inadequate information to provide reasonable assurance that such ingredient does not… |
| Initiation date | Jan 12, 2005 |
| City | Dallas |
| Country | United States |
| FEI number | 2510359 |
At a glance
- 1–9 Products in this recall
- 1–9 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