Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Vet
Pets & Animals/Pet Medications

Schering Corp: Various Veterinary Injectable and Ophthalmic Products Recalled for Sterility Issues

Agency Publication Date: January 17, 2003
Share:
Sign in to monitor this recall

Summary

Approximately 746,749 units of various veterinary medications manufactured by Schering Corp, including brands like Banamine, Nuflor, and Gentocin, are being recalled due to concerns regarding sterility assurance. The recall affects several types of sterile solutions used for injections in cattle, horses, dogs, and piglets, as well as ophthalmic ointments for eye treatments. These products were distributed nationwide through various distributors, hospitals, clinics, and veterinarians. Consumers should contact their veterinarian or the manufacturer immediately for instructions.

Risk

If a product intended to be sterile is contaminated, it can cause serious infections or abscesses at the injection site or in the eye, potentially leading to systemic illness or death in the treated animal.

What You Should Do

  1. Identify if you have any of the affected products: Garasol (80mL), Azium (100mL), Pro-Labs Flu-Nix (50mL, 100mL), Banamine (50mL, 100mL, 250mL), Betasone (5mL), Durvet Garacin Piglet (250mL), Gentocin Solution (100mL), Gentocin Ophthalmic Ointment (12-tube packs), or Nuflor (100mL, 250mL, 500mL).
  2. Check the specific Recall Numbers associated with these items: V-031-3 through V-040-3.
  3. Stop using these medications immediately and quarantine any remaining stock to ensure they are not administered to animals.
  4. Contact your veterinarian or healthcare provider to discuss alternative treatments and to report any adverse health events observed in treated animals.
  5. Return any unused product to the place of purchase or pharmacy for a refund and contact Schering Corp at their Galloping Hill Rd, Kenilworth, NJ location for further instructions.
  6. For additional questions, contact the FDA Veterinary Medicine hotline at 1-240-402-7002.

Your Remedy Options

๐Ÿ’ฐFull Refund

Veterinary drug refund

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

Affected Products

Product: Garasol Injection, (Gentamicin Sulfate), 100mg/mL (80 mL Vial)
Model:
Recall #: V-031-3
Product: Azium Injection Solution, 2mg/mL Dexamethasone (100mL Vial)
Model:
Recall #: V-032-3
Product: Pro-Labs Flu-Nix Injectable Solution, Flunixin meglumine equivalent to 50mg/mL (50 mL and 100mL Vials)
Model:
Recall #: V-033-3
Product: Banamine Injectable Solution, Flunixin meglumine equivalent to 50mg/mL (50mL, 100mL and 250mL Vials)
Model:
Recall #: V-034-3
Product: Betasone Aqueous Suspension, 5mg/mL Betamethasone diporpionate / 2mg/mL Betamethasone sodium phosphate (5mL Vial)
Model:
Recall #: V-035-3
Product: Durvet Garacin Piglet Injection, 5mg/mL Gentamicin base (250mL Vial)
Model:
Recall #: V-036-3
Product: Garacin Piglet Injection, 5mg/mL Gentamicin base (250mL Vial)
Model:
Recall #: V-037-3
Product: Gentocin Solution, 100mg/mL Gentamicin Base (100mL Vial)
Model:
Recall #: V-038-3
Product: Gentocin Ophthalmic Ointment, 3mg/mL Gentamicin base (1/8oz tubes, 12-pack)
Model:
Recall #: V-039-3
Product: Nuflor Injectable Solution, 300 mg/mL Florfenicol (100mL, 250mL, and 500mL Vials)
Model:
Recall #: V-040-3

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 25053
Status: Active
Manufacturer: Schering Corp
Sold By: distributors; hospitals; clinics; veterinarians; Durvet, Inc.; Pro Labs Ltd.; Agri Labs
Manufactured In: United States
Units Affected: 10 products (34776; 12944; 8700; 237161; 12630; 5338; 5385; 21861; 81864; 326090)
Distributed To: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, Wisconsin, Wyoming

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