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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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Low RiskFDA Vet
Pets & Animals/Pet Medications

Virbac AH, Inc: IVERHART Plus Flavored Chewables Recalled for Minocycline Contamination

Agency Publication Date: February 6, 2004
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Summary

Virbac AH, Inc. is recalling four lots of IVERHART Plus (ivermectin/pyrantel) Flavored Chewables, affecting approximately 18,500 display and tower units (nearly 1.2 million individual tablets). The medication is intended for heartworm prevention in dogs but was found to be contaminated with Minocycline, an FDA-approved human antibiotic that is not approved for use in animals. This recall affects three different dosage strengths sold in various states including Texas, California, Florida, and New York. Consumers should immediately stop using the product and consult their veterinarian or pharmacist for guidance.

Risk

The chewables are contaminated with Minocycline, a human drug that has not been evaluated or approved by the FDA for use in dogs or other animal species. Exposure to unapproved drugs in pets may lead to unknown side effects or interfere with the effectiveness of the heartworm prevention treatment.

What You Should Do

  1. Check your product packaging for IVERHART Plus (ivermectin/pyrantel) Flavored Chewables in 6-count packs.
  2. Verify if your product matches the affected dosage and codes: for dogs up to 25 lbs (Recall V-015-4, codes 0170DS or 0180TS), for dogs 26 to 50 lbs (Recall V-016-4, codes 0170DM or 0180TM), or for dogs 51 to 100 lbs (Recall V-017-4, codes 0170DL or 018TL).
  3. Immediately stop administering the chewables to your dog if they match the affected lot information.
  4. Contact your veterinarian or pharmacist for guidance regarding your dog's heartworm prevention schedule and to report any health concerns.
  5. Return any unused tablets to the pharmacy or place of purchase for a refund and contact Virbac AH, Inc. for further instructions.
  6. For additional questions, contact the FDA Center for Veterinary Medicine at 1-240-402-7002.

Your Remedy Options

๐Ÿ’ฐFull Refund

Veterinary drug return and refund

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

Affected Products

Product: IVERHART Plus (ivermectin/pyrantel) Flavored Chewables for dogs up to 25 lbs (6-count)
Model:
V-015-4
Lot Numbers:
0170DS
0180TS
Product: IVERHART Plus (ivermectin/pyrantel) Flavored Chewables for dogs 26 to 50 lbs (6-count)
Model:
V-016-4
Lot Numbers:
0170DM
0180TM
Product: IVERHART Plus (ivermectin/pyrantel) Flavored Chewables for dogs 51 to 100 lbs (6-count)
Model:
V-017-4
Lot Numbers:
0170DL
018TL

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 27756
Status: Active
Manufacturer: Virbac AH, Inc
Sold By: veterinary clinics; pharmacies
Manufactured In: United States
Units Affected: 3 products (0170DS: 7,306 display units (438,360 tablets), and 0180TS: 90 tower units (10,800 tablets); 0170DM: 3,981 display units (238,860 tablets), and 0180TM: 30 tower units (3,600 tablets); 0170DL: 7,257 display units (435,420 tablets), and 018TL: 440 tower units (52,800 tablets))
Distributed To: Texas, Hawaii, Missouri, Colorado, Minnesota, Iowa, Indiana, Wisconsin, California, New Mexico, Washington, Oklahoma, South Dakota, New York, Arizona, Florida, Mississippi, Puerto Rico

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