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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 Label Information

Agency Publication Date: April 9, 2026
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Summary

HUVEPHARMA EOOD is recalling 241 bags (approximately 12,050 pounds) of AMPROL 25% (amprolium) Type A Medicated Article. This veterinary medication, intended for use in chickens, turkeys, and pheasants, is being recalled because one bag was found to be missing the required lot number and expiration date. No incidents or injuries have been reported to date.

Risk

The absence of a lot number and expiration date on the packaging prevents users from identifying the specific production batch or ensuring the medication is still within its effective shelf life.

What You Should Do

  1. Identify the affected product by looking for AMPROL 25% (amprolium) Type A medicated article in 50-pound bags with the NDC number 23243-9561-5.
  2. Check the product packaging for lot number XSC442 with an expiration date of 30Jun2028 or for any bag missing this labeling information entirely.
  3. Stop using the recalled product immediately.
  4. Contact the manufacturer, HUVEPHARMA, or your distributor to arrange for the return or proper disposal of the medication.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 if you have additional questions regarding this recall.

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 (50lb)by HUVEPHARMA
Variants: Type A Medicated Article
Model:
956150
Lot Numbers:
XSC442 (Exp 30Jun2028)
NDC:
23243-9561-5

Intended for use in chickens, turkeys, and pheasants. NADA# 012-350.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98712
Status: Active
Manufacturer: HUVEPHARMA EOOD
Sold By: Authorized distributors
Manufactured In: Bulgaria
Units Affected: 241 bags @ 50.0 lbs each, 12,050.0 lbs
Distributed To: Nationwide
Agency Last Updated: April 21, 2026

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