Drug recall
AMPROL 25% (amprolium), Type A medicated article, Net Wt.: 50lb (22.68 kg), Manufactured by: HUVEPHARMA, INC…
FDA recall event 98712 · Class III · HUVEPHARMA EOOD
Key facts
| Event ID | 98712 |
|---|---|
| Recall numbers | V-0120-2026 |
| Recalling firm | HUVEPHARMA EOOD |
| Product type | Veterinary |
| Products | AMPROL 25% (amprolium), Type A medicated article, Net Wt.: 50lb (22.68 kg), Manufactured by: HUVEPHARMA, INC., St Louis, MO 63116, Distributed by: HUVEPHARMA, INC., Peachtree City, GA 30269. NADA#… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Missing lot number and expiration date on one (1) bag of material. |
| Initiation date | Apr 2, 2026 |
| Report date | Apr 15, 2026 |
| City | Sofia |
| Country | Bulgaria |
| FEI number | 3013203011 |
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 · Source date: