WhichRecall
Class IIReported 2025-11-26

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

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-0170-2026
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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