DermaRite Industries, LLC: Drug Recall
Recall #D-0170-2026 · 08/27/2025
Class II: Risk
Recall Details
- Recall Number
- D-0170-2026
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- DermaRite Industries, LLC
- Status
- Ongoing
- Date Initiated
- 08/27/2025
- Location
- North Bergen, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 57,837 units
Reason for Recall
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Product Description
Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
Distribution Pattern
Nationwide in the USA
Other Recalls by DermaRite Industries, LLC
- Class II: Risk 08/27/2025
- Class II: Risk 08/27/2025
- Class II: Risk 08/27/2025
- Class II: Risk 08/27/2025
- Class II: Risk 08/27/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.