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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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Low RiskFDA Vet
Pets & Animals/Pet Medications

AMPROL 25% Medicated Article Recalled for Missing Lot and Expiration Date

Agency Publication Date: December 16, 2024
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Summary

Huvepharma EAD is recalling 239 bags of AMPROL 25% (amprolium), a Type A medicated article used for livestock. The recall was initiated because the product packaging is missing the lot number and expiration date. Without this information, users cannot ensure the product is within its shelf life or identify if they have a specific batch affected by future safety or quality issues.

Risk

Missing lot numbers and expiration dates prevent proper tracking and monitoring of the medication's potency and safety over time. There is a low risk to animal health, but using expired medicated articles may result in sub-therapeutic dosing or ineffective treatment of the animals.

What You Should Do

  1. Identify your product by checking for 50 lb (22.68 kg) bags of AMPROL 25% (amprolium) manufactured by HUVEPHARMA, INC. with NADA: 012-350.
  2. Check the packaging for a lot number and expiration date; this recall specifically affects 239 bags of Lot WSC556 that are missing this information.
  3. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return or proper disposal.
  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: AMPROL 25% (amprolium), Type A medicated article (50 lb)by HUVEPHARMA
Lot Numbers:
WSC556

NADA: 012-350; Recall #: V-0047-2025; Missing lot number and expiration date on packaging.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95985
Status: Active
Manufacturer: Huvepharma EAD
Sold By: distributors; feed mills
Manufactured In: Bulgaria
Units Affected: 239 bags
Distributed To: Georgia, North Carolina, Tennessee
Agency Last Updated: December 20, 2024

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