DermaRite Industries, LLC recalls Lantiseptic
- Recalling company
- DermaRite Industries, LLC
- Product
- Lantiseptic, Dry Skin Therapy, Lanolin USP 30%, packaged in a) 5 g (0.17 oz) (NDC 61924-504-05), b) 4 oz (NDC 61924-504-04), and c)14 oz (NDC 61924-710-14) tubes, 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
- 8,378 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-0169-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0169-2026 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.