Gordofilm Wart Remover — Class II drug recall D-0495-2024
Completed recall by Dercher Enterprises, Inc., DBA Gordon Laboratories, reported 2024-05-22, distributed nationwide. cGMP Deviations
| Recall number | D-0495-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dercher Enterprises, Inc., DBA Gordon Laboratories, Upper Darby, PA, United States |
| Recall initiated | 2024-04-12 |
| Classified | 2024-05-13 |
| Reported by FDA | 2024-05-22 |
| Distributed | Nationwide (US) |
| Quantity | 5,247 glass |
| Reason classes | cgmp |
| NDC | 10481-3009-01 |
| Lot numbers | F135, F146 |
| Expiration dates | 2025-03-20, 2026-01-20, 2026-09-20 |
Product
Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, Gordon Laboratories, Upper Darby PA 19082, NDC 10481-3009-01
Reason for recall
cGMP Deviations
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0495-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.