Moderate riskFDA FoodClass II
BetaVet horse injectable recalled over defective vial seal
American Regent Inc. is recalling one lot of BetaVet, a betamethasone injectable suspension for intra-articular use in horses, sold in 5 mL single-dose vials. The vial crimps or seal may be loose or defective, which could affect the container's integrity. The recall covers lot 26038L2C1 (expires July 2027) and was distributed nationwide; no injuries have been reported.
From the FDA notice · Read the official notice ↗ · All American Regent recalls
What to do
- Check the lot number on your BetaVet vial for 26038L2C1 with expiration July 2027.
- Do not use vials from this lot.
- Contact your veterinarian or American Regent, Inc. for guidance on returns or replacement.
Is yours affected?
Compare your label or packaging with the recalled product.
- Product
- BetaVet - betamethasone sodium phosphate and betamethasone acetate injectable suspension, 6 mg betamethasone/mL, For Intra-Articular Use in Horses. Not for IV Use. Single Dose Vial, 1 Vial (5 mL), American Regent, Inc., Animal Health, Shirley, NY 11967, NADA # 141-418, NDC 10797-720-01.
- Sold in
- Nationwide
- Made for
- Pets
Details
- Illnesses reported
- None reported
- Manufactured in
- 4150 Lyman Dr, Hilliard, Ohio, United States
- Classification
- Class II
- Recall number
- V-0008-2027
In the FDA's words
- Description
- BetaVet - betamethasone sodium phosphate and betamethasone acetate injectable suspension, 6 mg betamethasone/mL, For Intra-Articular Use in Horses. Not for IV Use. Single Dose Vial, 1 Vial (5 mL), American Regent, Inc., Animal Health, Shirley, NY 11967, NADA # 141-418, NDC 10797-720-01. Defective container: loose/defective crimps/seal. Lot: 26038L2C1, Expires: July 2027 Distribution: Nationwide within the U.S.
- Hazard
- Defective container: loose/defective crimps/seal.