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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

Noromycin 300 LA (Oxytetracycline Injection) Recalled for Lack of Sterility

Agency Publication Date: July 2, 2025
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Summary

Norbrook Inc is recalling 7,380 units of Noromycin 300 LA (oxytetracycline injection), a prescription antibiotic used for livestock. The recall was initiated because there is a lack of assurance regarding the product's sterility, which could lead to infections at the injection site. Affected products include lot number 4501-600A with an expiration date of December 2026.

Risk

Non-sterile injectable medications can cause serious infections, abscesses, or systemic illness in treated animals. Using a compromised antibiotic may fail to treat the underlying condition while introducing new bacterial risks.

What You Should Do

  1. Stop using the recalled Noromycin 300 LA (oxytetracycline injection) immediately.
  2. Check the product packaging for lot number 4501-600A and an expiration date of December 2026 to see if your supply is affected.
  3. Contact Norbrook Inc or your distributor to arrange for the return or proper disposal of the recalled antibiotic.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for 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: Noromycin 300 LA (oxytetracycline injection) ANTIBIOTICby Noromycin
Lot Numbers:
4501-600A (Exp.: December 2026)

Manufactured by: Norbrook Laboratories Limited, Newry, Northern Ireland, NADA# 141-143.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97099
Status: Active
Manufacturer: Norbrook Inc
Sold By: authorized distributors
Manufactured In: United Kingdom, United States
Units Affected: 7380 units
Distributed To: Ohio, Minnesota, Nebraska, Missouri, Kansas
Agency Last Updated: July 14, 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