Gordofilm Wart Remover Recall: C.G.M.P. Deviations in Salicylic Acid Product
Gordon Laboratories recalls Gordofilm Wart Remover (16.7% salicylic acid) due to cGMP deviations. Products with specific lot numbers and expiration dates are affected. Consumers should check their product details.
Recall notice
cGMP Deviations
Contact the company
What happened, in plain English
Gordon Laboratories is recalling Gordofilm Wart Remover (salicylic acid 16.7% USP) in 15 cc glass jars because of cGMP deviations. This means the product may not meet quality standards, though serious injury risks are not specified in the recall. Read more at govinfonow.com/recall/32740-gordofilm-wart-remover-recall-c-g-m-p-deviations-in.
Source Summary by GovInfoNow · govinfonow.com/recall/32740-gordofilm-wart-remover-recall-c-g-m-p-deviations-in · Updated September 23, 2026 · FDA enforcement record: FDA #D-0495-2024
Cite this page
“Gordofilm Wart Remover Recall: C.G.M.P. Deviations in Salicylic Acid Product.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32740-gordofilm-wart-remover-recall-c-g-m-p-deviations-in. Based on FDA recall #D-0495-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0495-2024%22&limit=1).
Why it’s dangerous
The recall is due to cGMP deviations, which are quality control issues in manufacturing. This could mean the product may not be as safe or effective as it should be, but the recall does not specify serious injury risks.
Who’s affected
People who own or use Gordofilm Wart Remover in 15 cc glass jars with specific lot numbers and expiration dates are affected. Those with the product may be at risk if the product does not meet quality standards.
How to tell if you have this one
Check for the product name 'Gordofilm Wart Remover', 15 cc glass jars, and specific lot numbers: F135 (exp. March 2025), F146 (exp. April 2025), G103 (exp. January 2026), or G194 (exp. September 2026).
- Brand
Gordon Laboratories- Category
Drug
What to do — step by step
Check Product Details
Look for the lot numbers and expiration dates listed in the recall notice to determine if your product is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Product was distributed nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 40 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0495-2024 (April 12, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0495-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.