Why it was recalled
cGMP Deviations
Product description
Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, Gordon Laboratories, Upper Darby PA 19082, NDC 10481-3009-01
Lot numbers, UPCs & expiration codes
Lot #: F135, Exp. Date March 2025; F146, Exp. Date April , 2025; G103, Exp. Date January 2026; G194, Exp. Date September 2026
Where it was sold
Product was distributed nationwide within the United States
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0495-2024
- Classification
- Class II
- Status
- Completed
- Recall initiated
- Apr 12, 2024
- FDA report date
- May 22, 2024
- Quantity
- 5,247 glass jars
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Dercher Enterprises, Inc., DBA Gordon Laboratories
Original FDA data
Every field from FDA enforcement report D-0495-2024, exactly as published.
Show all FDA fields
- City
- Upper Darby
- State
- PA
- Status
- Completed
- Country
- United States
- Event ID
- 94355
- Address
- 6801 Ludlow St
- Code information
- Lot #: F135, Exp. Date March 2025; F146, Exp. Date April , 2025; G103, Exp. Date January 2026; G194, Exp. Date September 2026
- Postal code
- 19082-2408
- Report date
- May 22, 2024
- Product type
- Drugs
- Recall number
- D-0495-2024
- Classification
- Class II
- Recalling firm
- Dercher Enterprises, Inc., DBA Gordon Laboratories
- Product quantity
- 5,247 glass jars
- Reason for recall
- cGMP Deviations
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, Gordon Laboratories, Upper Darby PA 19082, NDC 10481-3009-01
- Distribution pattern
- Product was distributed nationwide within the United States
- Recall initiation date
- Apr 12, 2024
- Initial firm notification
- Letter
- Center classification date
- May 13, 2024