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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

CORID and AMPROL 128 Soluble Powder Recalled for Stability Failure

Agency Publication Date: September 26, 2025
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Summary

Huvepharma Inc. is recalling 13,680 pouches of CORID (amprolium) 20% Soluble Powder and AMPROL 128 (amprolium soluble powder) 20% Soluble Powder. These veterinary products are used as coccidiostats for livestock but have failed to meet the required stability specifications for their active ingredient assay. The recall affects several lots distributed across AL, AR, KS, MO, and WY with expiration dates in April, July, and September 2026.

Risk

The product's active ingredient levels failed to meet stability requirements, which can result in the medication being less effective than intended. This may lead to inadequate treatment or prevention of coccidiosis in animals.

What You Should Do

  1. Check your supply for CORID 20% Soluble Powder (10 oz pouches) with lot numbers WSE091, WSE092 (Exp 04/2026) or XSE003 (Exp 07/2026).
  2. Check your supply for AMPROL 128 (10 oz packets) with lot number 970915 (Exp 09/2026).
  3. Stop using the recalled product immediately.
  4. Contact Huvepharma Inc. or your distributor to arrange for the return or proper disposal of the affected 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

Manufacturer return or disposal coordination.

How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return or proper disposal.

Affected Products

Product: CORID (amprolium) 20% Soluble Powder Coccidiostat (10 oz)
Variants: 20% Soluble Powder
Lot Numbers:
WSE091 (Exp APR2026)
WSE092 (Exp APR2026)
XSE003 (Exp JUL2026)
NDC:
23243-9709-3

NADA #033-165; Recall #: V-0016-2026

Product: AMPROL 128 (amprolium soluble powder) 20% Soluble Powder Coccidiostat (10 oz)
Variants: 20% Soluble Powder, 24 packets per carton
Lot Numbers:
970915 (Exp SEP2026)
NDC:
23243-2309-3

NADA #033-165; Recall #: V-0017-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97637
Status: Active
Manufacturer: Huvepharma Inc.
Sold By: authorized distributors; veterinary suppliers
Manufactured In: United States
Units Affected: 13,680 pouches
Distributed To: Alabama, Arkansas, Kansas, Missouri, Wyoming
Agency Last Updated: November 25, 2025

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