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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

Banamine Transdermal (flunixin) Recalled for Bottle Leakage and Exposure Risk

Agency Publication Date: May 9, 2023
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Summary

Intervet, Inc. is recalling approximately 4,840 bottles of Banamine Transdermal (flunixin transdermal solution), a veterinary medication used for cattle. The recall was initiated because the product can leak between the cap and the bottle, creating a risk of unintended exposure to the medication for people handling the bottles or for the animals receiving treatment. While there have been no reports of injuries or illnesses related to this issue, the manufacturer is voluntarily removing the affected batch from the market.

Risk

The leakage between the cap and bottle can lead to skin or eye contact with the flunixin solution, which may cause irritation or other adverse health effects in humans and animals.

What You Should Do

  1. Check your supply for Banamine Transdermal (flunixin transdermal solution) in 250 mL bottles with NDC 0061-4363-02, Batch # 2664101, and an expiration date of May 2024.
  2. 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.
  3. 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: Banamine Transdermal (flunixin transdermal solution)
Variants: 250 mL bottle
Lot Numbers:
2664101 (Exp May 2024)
NDC:
0061-4363-02

Recall #: V-0120-2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92255
Status: Resolved
Manufacturer: Intervet, Inc
Sold By: veterinary distributors; nationwide retailers
Manufactured In: United States
Units Affected: 4,840 bottles
Distributed To: Nationwide
Agency Last Updated: May 15, 2023

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