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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 Drug
Medications & Supplements/Topical Products

Gordofilm Wart Remover Recalled for Manufacturing Practice Deviations

Agency Publication Date: May 13, 2024
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Summary

Dercher Enterprises, Inc., doing business as Gordon Laboratories, is recalling 5,247 glass jars of Gordofilm Wart Remover (salicylic acid 16.7% USP). The recall was initiated because of Current Good Manufacturing Practice (cGMP) deviations, meaning the product was not manufactured according to required quality standards. This medication, sold in 15 cc jars, was distributed nationwide to consumers who should contact a healthcare professional if they have used the product and have concerns.

Risk

Failure to follow Good Manufacturing Practices can lead to products that do not meet their quality, strength, or purity specifications. While no specific incidents have been reported, using a drug product that may be compromised poses a potential health risk to consumers.

What You Should Do

  1. This recall affects Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, identified by NDC 10481-3009-01.
  2. Check the product label for lot numbers F135 (Exp. March 2025), F146 (Exp. April 2025), G103 (Exp. January 2026), or G194 (Exp. September 2026).
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Gordon Laboratories for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Gordofilm Wart Remover (15 cc)
Variants: Salicylic acid 16.7% USP, Glass jars
Lot Numbers:
F135 (Exp. March 2025)
F146 (Exp. April 2025)
G103 (Exp. January 2026)
G194 (Exp. September 2026)
NDC:
10481-3009-01

Manufacturer: Gordon Laboratories, Upper Darby PA 19082.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94355
Status: Resolved
Manufacturer: Dercher Enterprises, Inc., DBA Gordon Laboratories
Sold By: Retailers nationwide
Manufactured In: United States
Units Affected: 5,247 glass jars
Distributed To: Nationwide

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

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.