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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

BioCox 60 Medicated Feed Article Recalled for Reduced Potency

Agency Publication Date: March 10, 2026
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Summary

Huvepharma EAD has recalled 80 bags of BioCox 60 Type A Medicated Article (salinomycin sodium), a medication used in commercial livestock feed. The recall was initiated because the product failed stability testing, meaning it may not maintain its required strength or potency over time. This recall affects 50-pound bags from a specific production lot distributed in Mississippi. Because this is a commercial medicated article, livestock producers should stop using the product and arrange for its return through their supplier.

Risk

The product does not meet potency specifications, which may result in ineffective treatment or prevention of coccidiosis in livestock. No injuries or animal health incidents have been reported to date.

What You Should Do

  1. Identify if you have the affected BioCox 60 Type A Medicated Article by checking for lot number HSK50067 and NDC number 23243-6807-5 printed on the 50 lb (22.68 kg) bags.
  2. Stop using the recalled product immediately for livestock feed formulation.
  3. Contact Huvepharma, Inc. or your distributor to arrange for the return or proper disposal of any remaining inventory from this lot.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 if you have additional questions or concerns.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return or proper disposal.

Affected Products

Product: BioCox 60 Type A Medicated Article (50 lbs)
Variants: 60g/lb, 50 lbs (22.68 kg) per bag
Model:
V-0104-2026
Lot Numbers:
HSK50067
NDC:
23243-6807-5

Distributed by: Huvepharma, Inc., Peachtree City, GA 30269

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98491
Status: Active
Manufacturer: Huvepharma EAD
Sold By: Huvepharma, Inc.
Manufactured In: Bulgaria
Units Affected: 80 bags
Distributed To: Mississippi
Agency Last Updated: March 18, 2026

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