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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 Cloudy Appearance

Agency Publication Date: September 22, 2021
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Summary

Norbrook Inc. has recalled approximately 7,214 vials of Noromycin 300 LA (oxytetracycline injection 300 mg/ml), a commercial livestock medication. The recall was initiated because some vials were observed to have a cloudy appearance instead of being clear. This recall affects 500 mL amber glass vials from batch 9502-90A that were distributed to veterinary suppliers in Kansas, Missouri, and North Carolina. No incidents or injuries have been reported to date.

Risk

The cloudy appearance indicates a potential quality defect or contamination in the injection fluid. Injecting a compromised or cloudy medication into livestock can lead to reduced efficacy of the drug or adverse local or systemic reactions in the animals.

What You Should Do

  1. Check your inventory for Noromycin 300 LA (oxytetracycline injection 300 mg/ml) in 500 mL amber glass vials with batch number 9502-90A and lot number 9502-90A.
  2. Stop using the recalled product immediately.
  3. Contact Norbrook Inc. or your distributor to arrange for the return or proper disposal of the affected vials.
  4. Call the FDA Center for Veterinary Medicine at 1-240-402-7002 for additional questions.

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 300 mg/ml) (500 mL)
Variants: 300 mg/ml
Model:
NADA 141-143
Lot Numbers:
9502-90A

Distributed in Amber Glass Vials; Recall #: V-0159-2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88644
Status: Resolved
Manufacturer: NORBROOK INC
Sold By: Norbrook, Inc.; veterinary distributors
Manufactured In: United States
Units Affected: 7,214 vials
Distributed To: Kansas, Missouri, North Carolina
Agency Last Updated: September 30, 2021

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