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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

Trilogic Pharma LLC: Clindoral Periodontal Filler Recalled for Potential Syringe Seal Issues

Agency Publication Date: October 15, 2020
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Summary

Trilogic Pharma LLC has recalled 6,768 units of Clindoral Periodontal Filler, a veterinary medication used for dental treatments in animals. The recall was initiated because the syringes used for the medication may have compromised seals, which can lead to a reduction in the product's shelf life. This issue affects specific lots (1253, 1302, and 1334) that were distributed across 25 U.S. states.

Risk

A compromised syringe seal may allow air or contaminants into the medication, potentially causing the filler to degrade or lose its effectiveness before its printed expiration date. This could result in inadequate treatment for an animal's periodontal condition.

What You Should Do

  1. Check your veterinary supplies for Clindoral Periodontal Filler syringes.
  2. Identify if your product is affected by looking for Lot Number 1253 (Exp. 06/19), Lot Number 1302 (Exp. 09/19), or Lot Number 1334 (Exp. 12/19).
  3. Contact your veterinarian or healthcare provider to determine if any unused product from these lots needs to be returned or replaced.
  4. Return any unused product to the place of purchase for a refund and contact Trilogic Pharma LLC for further instructions.
  5. For additional questions, contact the FDA Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

๐Ÿ’ฐFull Refund

Drug recall remedy

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

Affected Products

Product: Clindoral Periodontal Filler
Model:
V-0003-2021
Lot Numbers:
1253 (Exp. 06/19)
1302 (Exp. 09/19)
1334 (Exp. 12/19)
Date Ranges: Exp. 06/19, Exp. 09/19, Exp. 12/19

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86558
Status: Resolved
Manufacturer: Trilogic Pharma LLC
Sold By: Veterinary distributors
Manufactured In: United States
Units Affected: 6,768 Units
Distributed To: Alabama, California, Colorado, Florida, Georgia, Iowa, Idaho, Indiana, Kansas, Kentucky, Michigan, Minnesota, Mississippi, North Carolina, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, South Dakota, Texas, Virginia, Washington, Wisconsin
Agency Last Updated: October 21, 2020

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