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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 Recalled for Bottle Leakage

Agency Publication Date: July 6, 2023
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Summary

Intervet, Inc. is recalling 3,555 bottles of Banamine Transdermal (flunixin meglumine), a veterinary medication used for livestock. The recall was initiated due to reports of leakage between the bottle and the cap. This defect may lead to loss of product or exposure to the medication during handling. The affected product was distributed nationwide in 250 ml bottles.

Risk

The leakage between the cap and bottle can lead to unintended exposure to the medication for handlers or inaccurate dosing for animals if the product is compromised. No specific animal or human injuries have been reported in this notice.

What You Should Do

  1. Check your supply for Banamine Transdermal 250 ml bottles with NDC 0061-4363-02, Batch number 2706101, and an expiration date of June 2024.
  2. If you have animal health concerns or believe your livestock has been affected by a leaking bottle, contact your veterinarian.
  3. 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 if you have 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 (250 ml)
Variants: Transdermal solution
Model:
V-0139-2023
Lot Numbers:
2706101 (Exp June 2024)
NDC:
0061-4363-02

Recall initiated due to leakage between the cap and bottle.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92578
Status: Resolved
Manufacturer: Intervet, Inc
Sold By: Veterinary suppliers; Authorized distributors
Manufactured In: United States
Units Affected: 3,555 bottles
Distributed To: Nationwide
Agency Last Updated: July 12, 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