Drug recall
BetaVet, (Betamethasone Sodium Phosphate and Betamethasone Acetate Injectable Suspension), 6 mg betamethasone…
FDA recall event 97903 · Class II · American Regent Inc.
Key facts
| Event ID | 97903 |
|---|---|
| Recall numbers | V-0018-2026 |
| Recalling firm | American Regent Inc. |
| Product type | Veterinary |
| Products | BetaVet, (Betamethasone Sodium Phosphate and Betamethasone Acetate Injectable Suspension), 6 mg betamethasone per mL, Single Dose Vial, 1 Vial (6 mL), For Intra-Articular Use in Horses. Not for IV… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Lack of sterility assurance: Loose crimps/seals on vials. |
| Initiation date | Nov 4, 2025 |
| Report date | Dec 3, 2025 |
| City | Hilliard |
| State | OH |
| Country | United States |
| FEI number | 3005761472 |
At a glance
- 1–9 Products in this recall
- 10–99 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: