Recall D-0169-2026

US Class II Ongoing · initiated 2025-08-27

Recalling firm

DermaRite Industries, LLC, NJ

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 for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

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