Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Vet
Pets & Animals/Pet Medications

BetaVet Injectable Suspension Recalled for Lack of Sterility

Agency Publication Date: November 26, 2025
Share:
Sign in to monitor this recall

Summary

American Regent Inc. is recalling 17,234 vials of BetaVet (betamethasone sodium phosphate and betamethasone acetate injectable suspension) 6 mg/mL for horses. The recall was initiated because some vials were found to have loose seals or crimps, which means the medication may not be sterile. If the sterility of an injectable medication is compromised, it can lead to serious infections in the animal's joints.

Risk

Loose seals on medication vials can allow bacteria and other contaminants to enter the bottle, compromising the sterility of the injectable suspension. Injecting a non-sterile product into a horse's joint can cause severe joint infections and inflammation.

What You Should Do

  1. Identify the affected product by looking for BetaVet (betamethasone sodium phosphate and betamethasone acetate injectable suspension), 6 mg per mL, in a 6 mL single-dose vial.
  2. Check the packaging for lot number 25029L1C1.
  3. Stop using the recalled product immediately.
  4. If you have animal health concerns, contact your veterinarian. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer or supplier for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: If you have animal health concerns, contact your veterinarian. Return any unused product to the place of purchase for a refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: BetaVet (betamethasone sodium phosphate and betamethasone acetate injectable suspension) (6 mL)by American Regent Animal Health
Variants: 6 mg betamethasone per mL, Single Dose Vial, Injectable Suspension
Lot Numbers:
25029L1C1

Recall #: V-0018-2026; For Intra-Articular Use in Horses. Not for IV Use.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97903
Status: Active
Manufacturer: American Regent Inc.
Sold By: Veterinary suppliers; Wholesalers
Manufactured In: United States
Units Affected: 17,234 vials
Distributed To: Nationwide
Agency Last Updated: December 4, 2025

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response