CLASS II Drug recall · Reported 22 May 2024 · FDA Enforcement Report
Gordofilm Wart Remover (salicylic acid 7% USP) recalled
Dercher Enterprises, Inc is recalling Gordofilm Wart Remover (salicylic acid 7% USP), distributed nationwide in the US. The recall was initiated on 12 Apr 2024 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0495-2024
- FDA event ID
- 94355
- Recalling firm
- Dercher Enterprises, Inc, Upper Darby, PA
- Classification
- Class II
- Status
- Completed
- Recall initiated
- 12 Apr 2024
- FDA classified
- 13 May 2024
- Reported
- 22 May 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Foreign Material
Timeline
| 12 Apr 2024 | Recall initiated by company | |
| 13 May 2024 | Classified by FDA | +31 days |
| 22 May 2024 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
cGMP Deviations
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, Gordon Laboratories, Upper Darby PA 19082, NDC 10481-3009-01
Where it was distributed
Product was distributed nationwide within the United States
Questions about this recall
Is Gordofilm Wart Remover (salicylic acid 7% USP) recalled?
Yes. Dercher Enterprises, Inc recalled Gordofilm Wart Remover (salicylic acid 7% USP) on 12 Apr 2024. The recall is Class II and its status is Completed. Recall number D-0495-2024.
Why was it recalled?
cGMP Deviations
Which lots are affected?
Lot #: F135, Exp. Date March 2025; F146, Exp. Date April , 2025; G103, Exp. Date January 2026; G194, Exp. Date September 2026
Where was it sold?
Product was distributed nationwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Dercher Enterprises, Inc
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Monsel's (Ferric Subsulfate) Solution amber recalled | Dercher Enterprises, Inc | Foreign Material | Nationwide |