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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

Virbac AH, Inc: Suprelorin F Ferret Implants Recalled for Severe Temperature Exposure

Agency Publication Date: October 6, 2014
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Summary

Virbac AH, Inc. is recalling 120 units of Suprelorin F (deslorelin acetate) 4.7 mg Implants specifically for use in ferrets. These products were exposed to severe temperature excursions while being transported from Australia to the United States, which can damage the medication's effectiveness or safety. Because this is a veterinary drug product, you should contact your veterinarian or healthcare provider if your pet was treated with an implant from these specific lots. This product is only marketed for use in ferrets and must not be used in animals intended for human or animal food.

Risk

Severe temperature changes during transit can degrade the active ingredients or compromise the delivery mechanism of the implant. This may result in the product failing to work as intended or causing unforeseen health complications for the ferret.

What You Should Do

  1. Identify if you have the affected product by checking for Suprelorin F (deslorelin acetate) 4.7 mg Implants with lot numbers SCV281B21 or SCV281B51.
  2. Check the recall number V-006-2015 and the FDA Index number MIF 900-013 on the packaging to confirm the affected batch.
  3. If you are a veterinarian or pet owner in possession of an unused implant from these lots, do not administer it to any animal.
  4. Contact your veterinarian or healthcare provider immediately for guidance and to discuss potential health impacts if your ferret has already received an implant from these lots.
  5. Return any unused product to the place of purchase for a refund and contact Virbac AH, Inc. at 3200 Meacham Blvd, Fort Worth, Texas for further instructions.
  6. For additional questions or to report issues, contact the FDA Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

💰Full Refund

Veterinary drug refund and guidance

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

Affected Products

Product: Suprelorin F (deslorelin acetate) 4.7 mg Implant
Model:
MIF 900-013
V-006-2015
Lot Numbers:
SCV281B21
SCV281B51

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 69171
Status: Resolved
Manufacturer: Virbac AH, Inc
Sold By: Veterinary clinics; Specialty retailers
Manufactured In: Australia, United States
Units Affected: 120 Units
Distributed To: Alabama, Arizona, California, Colorado, Connecticut, Delaware, Illinois, Indiana, Iowa, Florida, Georgia, Kentucky, Louisiana, Maine, Maryland, Minnesota, Mississippi, Missouri, New Jersey, New Mexico, New York, North Dakota, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin

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 · Raw API Response