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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.

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Medium RiskFDA Vet
Pets & Animals/Pet Medications

Firocoxib Tablets for Horses Recalled Due to Dissolution Failure

Agency Publication Date: July 8, 2025
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Summary

Pegasus Laboratories, Inc. is recalling 2,664 bottles of Firocoxib Tablets for Horses (57mg) because the tablets did not meet quality standards for dissolution testing at the 120-minute mark. This failure means the medication may not break down correctly in the animal's system, potentially affecting its effectiveness. These tablets were distributed to two states, Pennsylvania and Ohio, in 60-count bottles.

Risk

The tablets failed to dissolve according to specifications during quality testing, which may result in the medication not being absorbed properly by the horse, potentially leading to inadequate treatment of the animal's condition.

What You Should Do

  1. Check your medication bottles for Firocoxib Tablets for Horses, 57mg, in 60-count bottles with NDC 49427-390-48.
  2. Verify if your bottle belongs to Lot 24289A1 with an expiration date of 08/26.
  3. 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.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

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: Firocoxib Tablets for Horses (60 Tablets)
Variants: 57mg, Tablet
Lot Numbers:
24289A1 (Exp: 08/26)
NDC:
49427-390-48

Recall Number: V-0102-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97098
Status: Active
Manufacturer: Pegasus Laboratories, Inc.
Sold By: Distributors
Manufactured In: United States
Units Affected: 2,664 bottles
Distributed To: Pennsylvania, Ohio
Agency Last Updated: July 15, 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