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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: Clintabs (clindamycin hydrochloride) Tablets Recalled for Missing Labeling

Agency Publication Date: January 23, 2015
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Summary

Virbac AH, Inc. is voluntarily recalling approximately 10,098 bottles of Clintabs (clindamycin hydrochloride) tablets because they were distributed without necessary product labeling. These prescription antibiotic tablets are intended for use in dogs only and are sold in 25 mg, 75 mg, and 150 mg strengths. Missing labels can lead to the improper administration of medication or the use of the drug for the wrong animal, which may result in ineffective treatment or adverse reactions. Consumers should check their pet's medication immediately to see if it is part of this recall.

Risk

Missing product labels mean critical dosing instructions, safety warnings, and usage information are unavailable, which could lead to medication errors or pet injury. While this is a low-risk recall, the absence of labeling prevents the safe and effective use of the prescription drug.

What You Should Do

  1. Check your dog's Clintabs (clindamycin hydrochloride) medication bottles for the following identifying details: 25 mg (NDC 051311-400-40), 75 mg (NDC 051311-402-75), or 150 mg (NDC 051311-404-15).
  2. Identify if your specific bottle is affected by checking the lot numbers and expiration dates: for 25 mg tablets, check for Lot 140129 (Exp 01/2016) or Lot 140294 (Exp 02/2016); for 75 mg tablets, check for Lot 140697 (Exp 06/2016); for 150 mg tablets, check for Lot 140955 (Exp 06/2016).
  3. Contact your veterinarian or pharmacist immediately if you possess a bottle that is missing its label or belongs to the affected lots to determine if your pet's treatment plan should be adjusted.
  4. Return any unused or mislabeled product to the pharmacy or veterinary clinic where it was purchased for a refund and contact Virbac AH, Inc. at their Fort Worth, TX headquarters for further instructions.
  5. For additional information or questions regarding this recall, contact the FDA Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

💰Full Refund

Contact healthcare provider and return product.

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

Affected Products

Product: Virbac Clintabs Tablets, clindamycin hydrochloride tablets, 25 mg (400-count bottles)
Model:
ANDA #200-316
NDC 051311-400-40
Recall #: V-213-2015
Lot Numbers:
140129 (Exp 01/2016)
140294 (Exp 02/2016)
Date Ranges: Expiration 01/2016, Expiration 02/2016
Product: Virbac Clintabs Tablets, clindamycin hydrochloride tablets, 75 mg (200-count bottles)
Model:
ANDA #200-316
NDC 051311-402-75
Recall #: V-214-2015
Lot Numbers:
140697 (Exp 06/2016)
Date Ranges: Expiration 06/2016
Product: Virbac Clintabs Tablets, clindamycin hydrochloride tablets, 150 mg (100-count bottles)
Model:
ANDA #200-316
NDC 051311-404-15
Recall #: V-215-2015
Lot Numbers:
140955 (Exp 06/2016)
Date Ranges: Expiration 06/2016

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 70031
Status: Resolved
Manufacturer: Virbac AH, Inc
Sold By: Veterinary clinics; Animal pharmacies
Manufactured In: United States
Units Affected: 3 products (8,034/400-count/bottles; 1152/200-count/bottles; 912/100-count/Bottles)
Distributed To: California, Colorado, Florida, Georgia, Iowa, Illinois, Indiana, Maryland, Michigan, Minnesota, Missouri, Mississippi, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Virginia, Wisconsin, 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 · Raw API Response