DermaRite Industries, LLC recalls Hand-E-Foam
- Recalling company
- DermaRite Industries, LLC
- Product
- Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
- Reason
- CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 27, 2025
- Reported
- Nov 26, 2025
- Distribution
- Nationwide in the USA
- Status
- Ongoing
- Quantity
- 576 containers
- Lot / codes
- All lots on or before expiry date 08/2027
- Company location
- North Bergen, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0167-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0167-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.