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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

IVX Animal Health Inc: Flunixin Meglumine Injection Recalled for Low pH Levels

Agency Publication Date: June 10, 2006
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Summary

IVX Animal Health Inc. is recalling 7,294 bottles of Flunixin Meglumine Injection 50 mg/mL, a prescription veterinary medication. The recall includes 250-mL bottles sold under the Aspen Veterinary Resources and AmTech Group labels. The medication was found to have a low pH level, which means the acidity of the liquid is outside of the required safety and stability specifications. This product was distributed to distributors in Nebraska, New Jersey, Colorado, California, Texas, Washington, and China.

Risk

A low pH level in an injectable medication can cause irritation or tissue damage at the site of injection and may affect the stability and effectiveness of the drug.

What You Should Do

  1. Check your supply for 250-mL bottles of Flunixin Meglumine Injection 50 mg/mL marketed under the 'Aspen Veterinary Resources, Ltd.' or 'AmTech Group, Inc.' labels.
  2. Verify if your product is affected by checking the label for ANDA 200-124 and noting if it was manufactured by Phoenix Scientific, Inc. or IVX Animal Health Inc.
  3. Immediately stop using any affected medication and secure it to prevent further administration to animals.
  4. Contact your veterinarian or pharmacist to discuss alternative treatments and to arrange for the return of the affected product.
  5. Contact IVX Animal Health Inc. at their Saint Joseph, Missouri office for specific instructions on how to return the unused product for a refund.
  6. For additional questions, contact the FDA Center for Veterinary Medicine at 1-240-402-7002.

Your Remedy Options

๐Ÿ’ฐFull Refund

Drug recall remedy

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

Affected Products

Product: Flunixin Meglumine Injection 50 mg/mL (250-mL bottle)
Model:
ANDA 200-124
V-077-6

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 35057
Status: Resolved
Manufacturer: IVX Animal Health Inc
Sold By: Aspen Veterinary Resources, Ltd.; AmTech Group, Inc.; distributors
Manufactured In: United States
Units Affected: 7,294 bottles
Distributed To: Nebraska, New Jersey, Colorado, California, Texas, Washington

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