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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

Huvepharma, Inc: Duramycin-10 (tetracycline hydrochloride) Recalled for Failed Stability

Agency Publication Date: December 27, 2016
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Summary

Huvepharma, Inc. has issued a voluntary recall for 14,876 bags of Duramycin-10 (tetracycline hydrochloride) soluble powder. This antibiotic, used for animal care, was found to have failed stability testing at the 48-month mark. The recall affects 6.4 oz (181g) packets sold nationwide in specific U.S. states.

Risk

The product's failure to maintain stability over its intended shelf life means the antibiotic may have reduced potency or effectiveness. This could lead to inadequate treatment of infections in animals being treated with the medication.

What You Should Do

  1. Check your supply of durvet Duramycin-10 (tetracycline hydrochloride) 6.4 oz (181g) packets for Lot # TSH20002.
  2. Verify the NDC number 30798-279-27 and the recall number V-0053-2017 located on the product packaging.
  3. Immediately stop using the affected lot of medication for animal treatment.
  4. Contact your veterinarian or healthcare provider for guidance regarding animals that have been treated with this product.
  5. Return any unused product to the place of purchase for a refund and contact Huvepharma, Inc. for further instructions.
  6. For additional questions, contact the FDA Center for Veterinary Medicine (CVM) at 240-402-7002.

Your Remedy Options

💰Full Refund

Voluntary field action/return

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: durvet Duramycin-10 Tetracycline Hydrochloride Soluble Powder (6.4 oz / 181g)
Model:
NDC: 30798-279-27
V-0053-2017
Lot Numbers:
TSH20002

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 75897
Status: Resolved
Manufacturer: Huvepharma, Inc
Sold By: Huvepharma, Inc; distributors
Manufactured In: United States
Units Affected: 14,876 bags
Distributed To: Alabama, Arkansas, California, Illinois, Louisiana, Texas, Kentucky, Indiana

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 · Raw API Response