WhichRecall
Class IIReported 2025-11-26

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.

Recalled by DermaRite Industries, LLC

Reason for Recall

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

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Recall Number
D-0169-2026
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-08-27
Reported
2025-11-26
Distribution
Nationwide in the USA
Code Info
All lots on or before expiry date 08/2027
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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