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.
Reported: November 26, 2025 Initiated: August 27, 2025 #D-0170-2026
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.
Reason for Recall
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Details
- Recalling Firm
- DermaRite Industries, LLC
- Units Affected
- 57,837 units
- Distribution
- Nationwide in the USA
- Location
- North Bergen, NJ
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by DermaRite Industries, LLC. Units affected: 57,837 units.
Why was this product recalled? ▼
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 26, 2025. Severity: Moderate. Recall number: D-0170-2026.
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