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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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High RiskFDA Vet
Pets & Animals/Pet Medications

IVX Animal Health Inc: Various Veterinary Injectable Medications Recalled for Sterility Failure

Agency Publication Date: February 7, 2006
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Summary

IVX Animal Health Inc. is recalling 74,217 units of various veterinary injectable medications, including GentaPoult (gentamicin sulfate), Oxytocin Injection, GentaMax 100, and Phenylbutazone 20% Injection. These products were manufactured on a processing line that experienced a sterility failure due to defective equipment. The recall affects 100-ml multi-dose vials sold under several brand names including AmTech, AgriLabs, Phoenix, Butler, VEDCO, VetTek, and RXV. Because these are injectable drugs that may not be sterile, they pose a significant health risk to the animals receiving them.

Risk

A failure in the sterilization process during manufacturing means these injectable drugs could be contaminated with bacteria or other microorganisms. Injecting a non-sterile product into an animal can cause serious infections, abscesses, or life-threatening systemic illness.

What You Should Do

  1. Identify if you have any of the affected 100-ml vials: AmTech GentaPoult (NDC 59130-742-01), AgriLabs Oxytocin, Phoenix GentaMax 100 (NDC 57319-286-05), Butler Gentamicin (NDC 11695-3536-1), VEDCO GentaVed 100 (NDC 50989-193-12), VetTek Gentamicin (NDC 60270-584-10), AgriLabs Legacy Gentamicin, RXV Gentamicin, Phenylbute Injection 20% (NDC 57319-339-05), or VEDCO Equi-Phar Phenylbutazone (NDC 50989-262-12).
  2. Immediately stop using any of these medications and quarantine them to prevent accidental administration to animals.
  3. Contact your veterinarian or pharmacist for guidance regarding the health of any animals that have recently received these injections.
  4. Return any unused product to the place of purchase for a refund or contact IVX Animal Health Inc at their Saint Joseph, MO location for further instructions.
  5. For additional questions, contact the FDA Center for Veterinary Medicine at 1-888-463-6332.

Your Remedy Options

๐Ÿ’ฐFull Refund

Refund for unused veterinary medication.

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

Affected Products

Product: AmTech Group, Inc. GentaPoult (Gentamicin Sulfate Injection) (100-ml)
Model:
ANADA 200-147
NDC 59130-742-01
Product: AgriLabs Oxytocin Injection (100-ml)
Model:
NADA 99-169
Product: Phoenix GentaMax 100 Gentamicin Sulfate Solution (100-ml)
Model:
ANADA 200-137
NDC 57319-286-05
Product: Butler Gentamicin Sulfate Solution (100-ml)
Model:
NDC 11695-3536-1
Product: VEDCO GentaVed 100 Gentamicin Sulfate Solution (100-ml)
Model:
NDC 50989-193-12
Product: VetTek Gentamicin Sulfate Solution (100-ml)
Model:
NDC 60270-584-10
Product: AgriLabs Legacy Gentamicin Sulfate Solution (100-ml)
Product: RXV Gentamicin Sulfate Solution (100-ml)
Product: Phenylbute Injection 20% (Phenylbutazone) (100-ml)
Model:
ANADA 200-126
NDC 57319-339-05
Product: VEDCO Equi-Phar Phenylbutazone Injection (100-ml)
Model:
NDC 50989-262-12

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 34264
Status: Resolved
Manufacturer: IVX Animal Health Inc
Sold By: veterinary drug distributors
Manufactured In: United States
Units Affected: 4 products (18,563/100-ml. vials; 28,438/100-ml. vials; 18,029/100-ml. vials; 9,187/100-ml. vials)
Distributed To: Missouri, Ohio, Texas, Georgia

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